Linked Data
dbSNP Id:
rs781473466
ExAC:
9:104187918 CAA / C
gnomAD v2:
9-104187918-CAA-C
gnomAD v4:
9-101425636-CAA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101425637_101425638del , CM000671.2:g.101425637_101425638del | GRCh38 |
| NC_000009.11:g.104187919_104187920del , CM000671.1:g.104187919_104187920del | GRCh37 |
| NC_000009.10:g.103227740_103227741del | NCBI36 |
| NG_012387.1:g.15143_15144del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647789.2:c.625-11_625-10del MANE Select | ENSP00000497767.1:n.625-11_625-10del | |
| ENST00000648064.1:c.625-11_625-10del | ENSP00000497990.1:n.625-11_625-10del | |
| ENST00000648758.1:c.625-11_625-10del | ENSP00000497731.1:n.625-11_625-10del | |
| ENST00000649902.1:c.625-11_625-10del | ENSP00000497216.1:n.625-11_625-10del | |
| ENST00000374855.8:c.625-11_625-10del | ENSP00000363988.4:n.625-11_625-10del | |
| ENST00000468981.3:n.152-11_152-10del | ||
| ENST00000616752.1:c.625-11_625-10del | ENSP00000481363.1:n.625-11_625-10del | |
| NM_000035.3:c.625-11_625-10del | NP_000026.2:n.625-11_625-10del | |
| NM_000035.4:c.625-11_625-10del MANE Select | NP_000026.2:n.625-11_625-10del |