Linked Data
ClinVar Variation Id:
133618
ClinVar RCV Id:
RCV000120136
RCV000129195
RCV000657024
RCV001355120
RCV001079506
RCV004551178
RCV003492517
dbSNP Id:
rs35184530
ExAC:
11:108155170 G / A
gnomAD v2:
11-108155170-G-A
gnomAD v3:
11-108284443-G-A
gnomAD v4:
11-108284443-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.108284443G>A , CM000673.2:g.108284443G>A | GRCh38 |
| NC_000011.9:g.108155170G>A , CM000673.1:g.108155170G>A | GRCh37 |
| NC_000011.8:g.107660380G>A | NCBI36 |
| NG_009830.1:g.66612G>A , LRG_135:g.66612G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452508.7:c.3963G>A | ENSP00000388058.2:p.Met1321Ile | |
| ENST00000713593.1:c.*3434G>A | ENSP00000518889.1:n.*3434G>A | |
| ENST00000278616.9:c.3963G>A | ENSP00000278616.4:p.Met1321Ile | |
| ENST00000682289.1:n.310G>A | ||
| ENST00000683174.1:n.4113G>A | ||
| ENST00000527805.6:c.3963G>A | ENSP00000435747.2:p.Met1321Ile | |
| ENST00000675595.1:c.3798G>A | ENSP00000502563.1:p.Met1266Ile | |
| ENST00000675843.1:c.3963G>A MANE Select | ENSP00000501606.1:p.Met1321Ile | |
| ENST00000278616.8:c.3963G>A | ENSP00000278616.4:p.Met1321Ile | |
| ENST00000452508.6:c.3963G>A | ENSP00000388058.2:p.Met1321Ile | |
| ENST00000527805.5:c.3963G>A | ENSP00000435747.1:p.Met1321Ile | |
| NM_000051.3:c.3963G>A , LRG_135t1:c.3963G>A | NP_000042.3:p.Met1321Ile | |
| XM_005271561.3:c.3963G>A | XP_005271618.2:p.Met1321Ile | |
| XM_005271562.3:c.3963G>A | XP_005271619.2:p.Met1321Ile | |
| XM_006718843.2:c.3963G>A | XP_006718906.1:p.Met1321Ile | |
| XM_011542840.1:c.3963G>A | XP_011541142.1:p.Met1321Ile | |
| XM_011542841.1:c.3963G>A | XP_011541143.1:p.Met1321Ile | |
| XM_011542842.1:c.3798G>A | XP_011541144.1:p.Met1266Ile | |
| XM_011542843.1:c.3963G>A | XP_011541145.1:p.Met1321Ile | |
| XM_011542844.1:c.2919G>A | XP_011541146.1:p.Met973Ile | |
| XM_011542845.1:c.2655G>A | XP_011541147.1:p.Met885Ile | |
| XM_011542846.1:c.3963G>A | XP_011541148.1:p.Met1321Ile | |
| NM_001351834.1:c.3963G>A | NP_001338763.1:p.Met1321Ile | |
| XM_005271562.5:c.3963G>A | XP_005271619.2:p.Met1321Ile | |
| XM_006718843.4:c.3963G>A | XP_006718906.1:p.Met1321Ile | |
| XM_011542840.3:c.3963G>A | XP_011541142.1:p.Met1321Ile | |
| XM_011542842.3:c.3798G>A | XP_011541144.1:p.Met1266Ile | |
| XM_011542843.2:c.3963G>A | XP_011541145.1:p.Met1321Ile | |
| XM_011542844.3:c.2919G>A | XP_011541146.1:p.Met973Ile | |
| XM_011542845.2:c.2655G>A | XP_011541147.1:p.Met885Ile | |
| XM_017017789.2:c.3963G>A | XP_016873278.1:p.Met1321Ile | |
| XM_017017790.2:c.3963G>A | XP_016873279.1:p.Met1321Ile | |
| XM_017017791.1:c.3963G>A | XP_016873280.1:p.Met1321Ile | |
| XM_017017792.2:c.3963G>A | XP_016873281.1:p.Met1321Ile | |
| XR_002957150.1:n.4696G>A | ||
| NM_001351834.2:c.3963G>A | NP_001338763.1:p.Met1321Ile | |
| NM_000051.4:c.3963G>A MANE Select | NP_000042.3:p.Met1321Ile |