Linked Data
ClinVar Variation Id:
1421852
dbSNP Id:
rs761810461
ExAC:
11:118963186 G / A
gnomAD v2:
11-118963186-G-A
gnomAD v3:
11-119092476-G-A
gnomAD v4:
11-119092476-G-A
COSMIC:
COSM923745
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.119092476G>A , CM000673.2:g.119092476G>A | GRCh38 |
| NC_000011.9:g.118963186G>A , CM000673.1:g.118963186G>A | GRCh37 |
| NC_000011.8:g.118468396G>A | NCBI36 |
| NG_008093.1:g.12600G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000686218.1:c.559G>A | ENSP00000509288.1:p.Glu187Lys | |
| ENST00000691144.1:n.2705G>A | ||
| ENST00000691249.1:n.1548G>A | ||
| ENST00000442944.7:c.706G>A | ENSP00000392041.3:p.Glu236Lys | |
| ENST00000536813.6:c.673G>A | ENSP00000438726.2:p.Glu225Lys | |
| ENST00000640813.1:c.534G>A | ENSP00000491061.1:p.Pro178= | |
| ENST00000648026.1:c.618G>A | ENSP00000498044.1:p.Pro206= | |
| ENST00000648374.1:c.673G>A | ENSP00000497255.1:p.Glu225Lys | |
| ENST00000649823.1:n.1181G>A | ||
| ENST00000650101.1:c.655G>A | ENSP00000496970.1:p.Glu219Lys | |
| ENST00000650307.1:n.1550G>A | ||
| ENST00000652429.1:c.724G>A MANE Select | ENSP00000498786.1:p.Glu242Lys | |
| ENST00000278715.7:c.724G>A | ENSP00000278715.3:p.Glu242Lys | |
| ENST00000392841.1:c.673G>A | ENSP00000376584.1:p.Glu225Lys | |
| ENST00000442944.6:c.673G>A | ENSP00000392041.2:p.Glu225Lys | |
| ENST00000537841.5:c.673G>A | ENSP00000444730.1:p.Glu225Lys | |
| ENST00000542044.5:n.1169G>A | ||
| ENST00000542729.5:c.601-282G>A | ENSP00000443058.1:n.601-282G>A | |
| ENST00000543090.5:c.631G>A | ENSP00000445429.1:p.Glu211Lys | |
| ENST00000543543.5:n.1199G>A | ||
| ENST00000544182.1:n.939G>A | ||
| ENST00000544387.5:c.652-282G>A | ENSP00000438424.1:n.652-282G>A | |
| ENST00000545621.5:c.*859G>A | ENSP00000444849.1:n.*859G>A | |
| ENST00000546226.5:n.1252G>A | ||
| NM_000190.3:c.724G>A | NP_000181.2:p.Glu242Lys | |
| NM_001024382.1:c.673G>A | NP_001019553.1:p.Glu225Lys | |
| NM_001258208.1:c.652-282G>A | NP_001245137.1:n.652-282G>A | |
| NM_001258209.1:c.601-282G>A | NP_001245138.1:n.601-282G>A | |
| XM_005271531.1:c.673G>A | XP_005271588.1:p.Glu225Lys | |
| XM_005271532.1:c.673G>A | XP_005271589.1:p.Glu225Lys | |
| XM_005271533.2:c.670G>A | XP_005271590.1:p.Glu224Lys | |
| XM_011542796.1:c.559G>A | XP_011541098.1:p.Glu187Lys | |
| NM_000190.4:c.724G>A MANE Select | NP_000181.2:p.Glu242Lys | |
| NM_001024382.2:c.673G>A | NP_001019553.1:p.Glu225Lys | |
| XM_005271533.3:c.670G>A | XP_005271590.1:p.Glu224Lys | |
| XM_017017629.1:c.673G>A | XP_016873118.1:p.Glu225Lys | |
| XM_024448460.1:c.598-282G>A | XP_024304228.1:n.598-282G>A | |
| NM_001258208.2:c.652-282G>A | NP_001245137.1:n.652-282G>A | |
| NM_001258209.2:c.601-282G>A | NP_001245138.1:n.601-282G>A |