Linked Data
dbSNP Id:
rs1172437013
gnomAD v3:
11-108256154-A-ATAT
gnomAD v4:
11-108256154-A-ATAT
MyVariant Identifiers:
chr11:g.108126881_108126882insTAT (hg19)
chr11:g.108256154_108256155insTAT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108256154_108256155insTAT , CM000673.2:g.108256154_108256155insTAT | GRCh38 |
| NC_000011.9:g.108126881_108126882insTAT , CM000673.1:g.108126881_108126882insTAT | GRCh37 |
| NC_000011.8:g.107632091_107632092insTAT | NCBI36 |
| NG_009830.1:g.38323_38324insTAT , LRG_135:g.38323_38324insTAT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000452508.7:c.2125-61_2125-60insTAT | ENSP00000388058.2:n.2125-61_2125-60insTAT... | |
| ENST00000713593.1:c.*1596-61_*1596-60insTAT | ENSP00000518889.1:n.*1596-61_*1596-60insT... | |
| ENST00000278616.9:c.2125-61_2125-60insTAT | ENSP00000278616.4:n.2125-61_2125-60insTAT... | |
| ENST00000682516.1:n.2259-61_2259-60insTAT | ||
| ENST00000683174.1:n.2275-61_2275-60insTAT | ||
| ENST00000683605.1:n.1620-61_1620-60insTAT | ||
| ENST00000684037.1:c.*1060-61_*1060-60insTAT | ENSP00000508245.1:n.*1060-61_*1060-60insT... | |
| ENST00000684061.1:n.2259-61_2259-60insTAT | ||
| ENST00000527805.6:c.2125-61_2125-60insTAT | ENSP00000435747.2:n.2125-61_2125-60insTAT... | |
| ENST00000675595.1:c.1960-61_1960-60insTAT | ENSP00000502563.1:n.1960-61_1960-60insTAT... | |
| ENST00000675843.1:c.2125-61_2125-60insTAT MANE Select | ENSP00000501606.1:n.2125-61_2125-60insTAT... | |
| ENST00000278616.8:c.2125-61_2125-60insTAT | ENSP00000278616.4:n.2125-61_2125-60insTAT... | |
| ENST00000452508.6:c.2125-61_2125-60insTAT | ENSP00000388058.2:n.2125-61_2125-60insTAT... | |
| ENST00000527805.5:c.2125-61_2125-60insTAT | ENSP00000435747.1:n.2125-61_2125-60insTAT... | |
| NM_000051.3:c.2125-61_2125-60insTAT , LRG_135t1:c.2125-61_2125-60insTAT | NP_000042.3:n.2125-61_2125-60insTAT | |
| XM_005271561.3:c.2125-61_2125-60insTAT | XP_005271618.2:n.2125-61_2125-60insTAT | |
| XM_005271562.3:c.2125-61_2125-60insTAT | XP_005271619.2:n.2125-61_2125-60insTAT | |
| XM_006718843.2:c.2125-61_2125-60insTAT | XP_006718906.1:n.2125-61_2125-60insTAT | |
| XM_011542840.1:c.2125-61_2125-60insTAT | XP_011541142.1:n.2125-61_2125-60insTAT | |
| XM_011542841.1:c.2125-61_2125-60insTAT | XP_011541143.1:n.2125-61_2125-60insTAT | |
| XM_011542842.1:c.1960-61_1960-60insTAT | XP_011541144.1:n.1960-61_1960-60insTAT | |
| XM_011542843.1:c.2125-61_2125-60insTAT | XP_011541145.1:n.2125-61_2125-60insTAT | |
| XM_011542844.1:c.1081-61_1081-60insTAT | XP_011541146.1:n.1081-61_1081-60insTAT | |
| XM_011542845.1:c.817-61_817-60insTAT | XP_011541147.1:n.817-61_817-60insTAT | |
| XM_011542846.1:c.2125-61_2125-60insTAT | XP_011541148.1:n.2125-61_2125-60insTAT | |
| NM_001351834.1:c.2125-61_2125-60insTAT | NP_001338763.1:n.2125-61_2125-60insTAT | |
| XM_005271562.5:c.2125-61_2125-60insTAT | XP_005271619.2:n.2125-61_2125-60insTAT | |
| XM_006718843.4:c.2125-61_2125-60insTAT | XP_006718906.1:n.2125-61_2125-60insTAT | |
| XM_011542840.3:c.2125-61_2125-60insTAT | XP_011541142.1:n.2125-61_2125-60insTAT | |
| XM_011542842.3:c.1960-61_1960-60insTAT | XP_011541144.1:n.1960-61_1960-60insTAT | |
| XM_011542843.2:c.2125-61_2125-60insTAT | XP_011541145.1:n.2125-61_2125-60insTAT | |
| XM_011542844.3:c.1081-61_1081-60insTAT | XP_011541146.1:n.1081-61_1081-60insTAT | |
| XM_011542845.2:c.817-61_817-60insTAT | XP_011541147.1:n.817-61_817-60insTAT | |
| XM_017017789.2:c.2125-61_2125-60insTAT | XP_016873278.1:n.2125-61_2125-60insTAT | |
| XM_017017790.2:c.2125-61_2125-60insTAT | XP_016873279.1:n.2125-61_2125-60insTAT | |
| XM_017017791.1:c.2125-61_2125-60insTAT | XP_016873280.1:n.2125-61_2125-60insTAT | |
| XM_017017792.2:c.2125-61_2125-60insTAT | XP_016873281.1:n.2125-61_2125-60insTAT | |
| XR_002957150.1:n.2858-61_2858-60insTAT | ||
| NM_001351834.2:c.2125-61_2125-60insTAT | NP_001338763.1:n.2125-61_2125-60insTAT | |
| NM_000051.4:c.2125-61_2125-60insTAT MANE Select | NP_000042.3:n.2125-61_2125-60insTAT |