Assay Details
Target Gene Details
Entrez Gene ID: | 8775 |
Gene Name: | NSF attachment protein alpha |
Gene Aliases: |
SNAPA |
Location: |
Chr.19:47487634-47515258 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NAPA | NM_003827.3 | 11 | 1508 | NP_003818.2 |
NR_038456.1 | ||||
NR_038457.1 | 9 | 1311 | ||
XM_011527436.1 | 11 | 1182 | XP_011525738.1 | |
XM_011527437.1 | 10 | 1261 | XP_011525739.1 | |
AA542963.1 | ||||
AA807920.1 | ||||
AK098401.1 | 11 | 1341 | ||
AK123456.1 | 1 | 1534 | ||
AK126519.1 | 5 | 3550 | ||
AW206113.1 | ||||
BC001165.1 | 11 | 1280 | AAH01165.1 | |
BC007432.2 | 11 | 1271 | AAH07432.1 | |
BC028234.1 | 11 | 1326 | AAH28234.1 | |
BC091511.1 | 11 | 1287 | AAH91511.1 | |
BU168063.1 | 6 | 746 | ||
U39412.1 | AAC80170.1 |
Target Gene Details
Entrez Gene ID: | 100505681 |
Gene Name: | NAPA antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.19:47484282-47501597 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NAPA-AS1 | NR_038452.1 | |||
AK057858.1 | ||||
BG035979.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2758765 | Chr.19:47354499 - 47522248 on Build GRCh38 | Loss | SLC8A2 NAPA-AS1 MEIS3 ZNF541 KPTN DHX34 NAPA |
nsv1056887 | Chr.19:47481963 - 47527369 on Build GRCh38 | Gain | NAPA-AS1 ZNF541 KPTN NAPA |
nsv953591 | Chr.19:47486744 - 47500943 on Build GRCh38 | Deletion | NAPA-AS1 KPTN NAPA |
nsv579888 | Chr.19:47428355 - 47658874 on Build GRCh38 | Gain | SLC8A2 NAPA-AS1 ZNF541 KPTN NAPA GLTSCR1 |
More Information
Additional Information:
For this assay, SNP(s) [rs114963766,rs73940857] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic Exonic Intronic Non-exonic DGV Variation |