Linked Data
ClinVar Variation Id:
302251
dbSNP Id:
rs199888434
gnomAD v2:
11-108168081-A-T
gnomAD v4:
11-108297354-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108297354A>T , CM000673.2:g.108297354A>T | GRCh38 |
| NC_000011.9:g.108168081A>T , CM000673.1:g.108168081A>T | GRCh37 |
| NC_000011.8:g.107673291A>T | NCBI36 |
| NG_009830.1:g.79523A>T , LRG_135:g.79523A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.4977A>T | ENSP00000388058.2:p.Ile1659= | |
| ENST00000713593.1:c.*4448A>T | ENSP00000518889.1:n.*4448A>T | |
| ENST00000278616.9:c.4977A>T | ENSP00000278616.4:p.Ile1659= | |
| ENST00000683174.1:n.6461A>T | ||
| ENST00000683524.1:n.201A>T | ||
| ENST00000684152.1:n.691A>T | ||
| ENST00000527805.6:c.*41A>T | ENSP00000435747.2:n.*41A>T | |
| ENST00000675595.1:c.*41A>T | ENSP00000502563.1:n.*41A>T | |
| ENST00000675843.1:c.4977A>T MANE Select | ENSP00000501606.1:p.Ile1659= | |
| ENST00000278616.8:c.4977A>T | ENSP00000278616.4:p.Ile1659= | |
| ENST00000452508.6:c.4977A>T | ENSP00000388058.2:p.Ile1659= | |
| ENST00000524792.5:n.1192A>T | ||
| ENST00000533690.5:n.381A>T | ||
| NM_000051.3:c.4977A>T , LRG_135t1:c.4977A>T | NP_000042.3:p.Ile1659= | |
| XM_005271561.3:c.4977A>T | XP_005271618.2:p.Ile1659= | |
| XM_005271562.3:c.4977A>T | XP_005271619.2:p.Ile1659= | |
| XM_006718843.2:c.4977A>T | XP_006718906.1:p.Ile1659= | |
| XM_006718845.1:c.933A>T | XP_006718908.1:p.Ile311= | |
| XM_011542840.1:c.4977A>T | XP_011541142.1:p.Ile1659= | |
| XM_011542841.1:c.4977A>T | XP_011541143.1:p.Ile1659= | |
| XM_011542842.1:c.4812A>T | XP_011541144.1:p.Ile1604= | |
| XM_011542843.1:c.4977A>T | XP_011541145.1:p.Ile1659= | |
| XM_011542844.1:c.3933A>T | XP_011541146.1:p.Ile1311= | |
| XM_011542845.1:c.3669A>T | XP_011541147.1:p.Ile1223= | |
| XM_011542846.1:c.4977A>T | XP_011541148.1:p.Ile1659= | |
| XM_011542847.1:c.48A>T | XP_011541149.1:p.Ile16= | |
| NM_001351834.1:c.4977A>T | NP_001338763.1:p.Ile1659= | |
| XM_005271562.5:c.4977A>T | XP_005271619.2:p.Ile1659= | |
| XM_006718843.4:c.4977A>T | XP_006718906.1:p.Ile1659= | |
| XM_006718845.2:c.933A>T | XP_006718908.1:p.Ile311= | |
| XM_011542840.3:c.4977A>T | XP_011541142.1:p.Ile1659= | |
| XM_011542842.3:c.4812A>T | XP_011541144.1:p.Ile1604= | |
| XM_011542843.2:c.4977A>T | XP_011541145.1:p.Ile1659= | |
| XM_011542844.3:c.3933A>T | XP_011541146.1:p.Ile1311= | |
| XM_011542845.2:c.3669A>T | XP_011541147.1:p.Ile1223= | |
| XM_017017789.2:c.4977A>T | XP_016873278.1:p.Ile1659= | |
| XM_017017790.2:c.4977A>T | XP_016873279.1:p.Ile1659= | |
| XM_017017791.1:c.4977A>T | XP_016873280.1:p.Ile1659= | |
| XM_017017792.2:c.4977A>T | XP_016873281.1:p.Ile1659= | |
| XR_002957150.1:n.5577A>T | ||
| NM_001351834.2:c.4977A>T | NP_001338763.1:p.Ile1659= | |
| NM_000051.4:c.4977A>T MANE Select | NP_000042.3:p.Ile1659= |