Assay Details
Target Gene Details
Entrez Gene ID: | 3265 |
Gene Name: | HRas proto-oncogene, GTPase |
Gene Aliases: |
C-BAS/HAS, C-H-RAS, C-HA-RAS1, CTLO, H-RASIDX, HAMSV, HRAS1, RASH1, p21ras |
Location: |
Chr.11:532242-535567 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
HRAS | NM_001130442.2 | 5 | 769 | NP_001123914.1 |
NM_001318054.1 | NP_001304983.1 | |||
NM_005343.3 | NP_005334.1 | |||
NM_176795.4 | 6 | 851 | NP_789765.1 | |
AB451336.1 | ||||
AB451485.1 | ||||
AF493916.1 | AAM12630.1 | |||
BC006499.2 | AAH06499.1 | |||
BC095471.1 | AAH95471.1 | |||
BM801600.1 | ||||
BM801632.1 | ||||
BQ574535.1 | 1 | 418 | ||
BQ674260.1 | 5 | 709 | ||
BT019421.1 | AAV38228.1 | |||
CR536579.1 | CAG38816.1 | |||
CR542271.1 | CAG47067.1 | |||
KJ534867.1 | ||||
KJ534868.1 |
Target Gene Details
Entrez Gene ID: | 115399 |
Gene Name: | leucine rich repeat containing 56 |
Gene Aliases: |
- |
Location: |
Chr.11:518967-554916 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LRRC56 | XM_011519875.2 | XP_011518177.1 | ||
XM_011519877.2 | XP_011518179.1 | |||
XM_017017167.1 | XP_016872656.1 | |||
XM_017017168.1 | XP_016872657.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv467634 | Chr.11:511805 - 619789 on Build GRCh38 | Loss | LRRC56 LMNTD2 LOC143666 MIR210HG LOC101059906 PHRF1 IRF7 MIR210 RASSF7 CDHR5 HRAS |
nsv527327 | Chr.11:295343 - 620599 on Build GRCh38 | Loss | LMNTD2 B4GALNT4 LOC143666 PKP3 IFITM3 LOC101059906 IRF7 PTDSS2 MIR210 SIGIRR CDHR5 RNH1 HRAS LRRC56 IFITM2 MIR210HG IFITM5 PHRF1 ANO9 PGGHG RASSF7 IFITM1 |
nsv951270 | Chr.11:528401 - 628100 on Build GRCh38 | Deletion | LRRC56 LMNTD2 LOC143666 MIR210HG LOC101059906 PHRF1 IRF7 SCT MIR210 RASSF7 CDHR5 HRAS |
nsv469923 | Chr.11:378188 - 1302334 on Build GRCh38 | Loss | B4GALNT4 LOC143666 AP2A2 TALDO1 IRF7 MIR6744 PTDSS2 MIR210 MUC6 SIGIRR MUC5AC RPLP2 HRAS LRRC56 CEND1 DRD4 CD151 CHID1 MIR210HG PDDC1 DEAF1 LMNTD2 TOLLIP POLR2L TSPAN4 SNORA52 PKP3 LOC101059906 SCT TMEM80 MUC2 CDHR5 PNPLA2 RNH1 PANO1 MUC5B PIDD1 SLC25A22 PHRF1 ANO9 EPS8L2 RASSF7 LOC101927503 LOC171391 CRACR2B |
esv2759794 | Chr.11:409846 - 1336162 on Build GRCh38 | Loss | TOLLIP-AS1 LOC143666 AP2A2 TALDO1 IRF7 MIR6744 PTDSS2 MIR210 MUC6 SIGIRR MUC5AC RPLP2 HRAS LRRC56 CEND1 DRD4 CD151 CHID1 MIR210HG PDDC1 DEAF1 LMNTD2 TOLLIP POLR2L TSPAN4 SNORA52 LOC101059906 SCT TMEM80 MUC2 CDHR5 PNPLA2 RNH1 PANO1 MUC5B PIDD1 SLC25A22 PHRF1 ANO9 EPS8L2 RASSF7 LOC101927503 LOC171391 CRACR2B |
nsv1053964 | Chr.11:491334 - 692433 on Build GRCh38 | Gain | LMNTD2 LOC143666 LOC101059906 IRF7 SCT PTDSS2 MIR210 CDHR5 RNH1 HRAS LRRC56 DRD4 MIR210HG PHRF1 RASSF7 DEAF1 |
dgv182e199 | Chr.11:349830 - 943372 on Build GRCh38 | Deletion | B4GALNT4 LOC143666 AP2A2 TALDO1 IRF7 PTDSS2 MIR210 SIGIRR RPLP2 HRAS LRRC56 CEND1 DRD4 CD151 CHID1 MIR210HG PDDC1 DEAF1 LMNTD2 POLR2L TSPAN4 SNORA52 PKP3 LOC101059906 SCT TMEM80 CDHR5 PNPLA2 RNH1 PANO1 PIDD1 SLC25A22 PHRF1 ANO9 EPS8L2 RASSF7 LOC171391 CRACR2B |
nsv1159791 | Chr.11:461793 - 909492 on Build GRCh38 | Deletion | LOC143666 TALDO1 IRF7 PTDSS2 MIR210 RPLP2 HRAS LRRC56 CEND1 DRD4 CD151 CHID1 MIR210HG PDDC1 DEAF1 LMNTD2 POLR2L TSPAN4 SNORA52 LOC101059906 SCT TMEM80 CDHR5 PNPLA2 RNH1 PANO1 PIDD1 SLC25A22 PHRF1 EPS8L2 RASSF7 LOC171391 CRACR2B |
More Information
Set Membership: |
Intragenic Exonic Intronic Non-exonic DGV Variation |