Linked Data
ClinVar Variation Id:
364376
dbSNP Id:
rs762785983
ExAC:
9:107546579 CG / C
gnomAD v2:
9-107546579-CG-C
gnomAD v3:
9-104784298-CG-C
gnomAD v4:
9-104784298-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.104784299del , CM000671.2:g.104784299del | GRCh38 |
| NC_000009.11:g.107546580del , CM000671.1:g.107546580del | GRCh37 |
| NC_000009.10:g.106586401del | NCBI36 |
| NG_007981.1:g.148857del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000374736.8:c.*16del MANE Select | ENSP00000363868.3:n.*16del | |
| ENST00000678995.1:c.*16del | ENSP00000504612.1:n.*16del | |
| ENST00000374736.7:c.*16del | ENSP00000363868.3:n.*16del | |
| NM_005502.3:c.*16del | NP_005493.2:n.*16del | |
| XM_005251773.1:c.*16del | XP_005251830.1:n.*16del | |
| XM_005251776.1:c.*16del | XP_005251833.1:n.*16del | |
| XM_011518339.1:c.*16del | XP_011516641.1:n.*16del | |
| XM_011518340.1:c.*16del | XP_011516642.1:n.*16del | |
| XM_011518341.1:c.*16del | XP_011516643.1:n.*16del | |
| XM_011518342.1:c.*16del | XP_011516644.1:n.*16del | |
| XM_005251773.3:c.*16del | XP_005251830.1:n.*16del | |
| XM_005251776.3:c.*16del | XP_005251833.1:n.*16del | |
| XM_011518339.3:c.*16del | XP_011516641.1:n.*16del | |
| XM_011518340.3:c.*16del | XP_011516642.1:n.*16del | |
| XM_011518341.3:c.*16del | XP_011516643.1:n.*16del | |
| XM_011518342.3:c.*16del | XP_011516644.1:n.*16del | |
| XM_017014378.2:c.*16del | XP_016869867.1:n.*16del | |
| XM_017014379.2:c.*16del | XP_016869868.1:n.*16del | |
| XM_017014380.2:c.*16del | XP_016869869.1:n.*16del | |
| XM_017014381.2:c.*16del | XP_016869870.1:n.*16del | |
| XM_017014382.2:c.*16del | XP_016869871.1:n.*16del | |
| NM_005502.4:c.*16del MANE Select | NP_005493.2:n.*16del |