Assay Details
Target Gene Details
Entrez Gene ID: | 84941 |
Gene Name: | hematopoietic SH2 domain containing |
Gene Aliases: |
ALX, HSH2 |
Location: |
Chr.19:16134028-16158575 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 2 - Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
HSH2D | NM_001291274.1 | NP_001278203.1 | ||
NM_032855.3 | NP_116244.1 | |||
NR_111903.1 | ||||
NR_111904.1 | ||||
XM_011528386.2 | XP_011526688.1 | |||
XM_011528387.2 | XP_011526689.1 | |||
XM_011528389.2 | XP_011526691.1 | |||
XM_011528390.1 | XP_011526692.1 | |||
XM_017027402.1 | XP_016882891.1 | |||
XM_017027403.1 | XP_016882892.1 | |||
XM_017027404.1 | XP_016882893.1 | |||
AK027792.1 | BAB55372.1 | |||
AK131222.1 | BAD18408.1 | |||
AK300027.1 | ||||
AY319652.1 | AAQ81285.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833767 | Chr.19:16121391 - 16347760 on Build GRCh38 | Loss | AP1M1 FAM32A CIB3 RAB8A HSH2D KLF2 |
esv3643789 | Chr.19:16141633 - 16146766 on Build GRCh38 | Loss | HSH2D |
More Information
Set Membership: |
Intragenic Non-exonic DGV Variation |