Linked Data
ClinVar Variation Id:
1005567
dbSNP Id:
rs778410642
ExAC:
11:6637976 G / A
gnomAD v2:
11-6637976-G-A
gnomAD v3:
11-6616745-G-A
gnomAD v4:
11-6616745-G-A
COSMIC:
COSM3810150
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6616745G>A , CM000673.2:g.6616745G>A | GRCh38 |
| NC_000011.9:g.6637976G>A , CM000673.1:g.6637976G>A | GRCh37 |
| NC_000011.8:g.6594552G>A | NCBI36 |
| NG_008653.1:g.7717C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682424.1:c.688C>T | ENSP00000507321.1:p.Arg230Trp | |
| ENST00000299427.12:c.802C>T MANE Select | ENSP00000299427.6:p.Arg268Trp | |
| ENST00000436873.7:c.312+556C>T | ||
| ENST00000524788.2:n.1961C>T | ||
| ENST00000524903.2:n.2077C>T | ||
| ENST00000528807.2:n.458C>T | ||
| ENST00000530040.2:n.480-242C>T | ||
| ENST00000533371.6:c.73C>T | ENSP00000437066.1:p.Arg25Trp | |
| ENST00000642892.1:c.73C>T | ENSP00000494165.1:p.Arg25Trp | |
| ENST00000643439.1:c.*542C>T | ENSP00000495849.1:n.*542C>T | |
| ENST00000643479.1:n.831C>T | ||
| ENST00000643516.1:c.396-242C>T | ||
| ENST00000644151.1:n.2241C>T | ||
| ENST00000644218.1:c.802C>T | ENSP00000493574.1:p.Arg268Trp | |
| ENST00000644683.1:c.*255C>T | ENSP00000494085.1:n.*255C>T | |
| ENST00000644810.1:c.523C>T | ENSP00000495895.1:p.Arg175Trp | |
| ENST00000644831.1:n.978C>T | ||
| ENST00000644933.1:c.73C>T | ENSP00000496133.1:p.Arg25Trp | |
| ENST00000645020.1:n.2092C>T | ||
| ENST00000645285.1:c.73C>T | ENSP00000495058.1:p.Arg25Trp | |
| ENST00000645331.1:n.1168C>T | ||
| ENST00000645620.1:c.73C>T | ENSP00000493657.1:p.Arg25Trp | |
| ENST00000646777.1:n.978C>T | ||
| ENST00000647016.1:n.1282C>T | ||
| ENST00000647152.1:c.73C>T | ENSP00000495893.1:p.Arg25Trp | |
| ENST00000647209.1:c.*671C>T | ENSP00000495558.1:n.*671C>T | |
| ENST00000647346.1:n.1822C>T | ||
| ENST00000299427.10:c.802C>T | ENSP00000299427.6:p.Arg268Trp | |
| ENST00000436873.6:c.451-242C>T | ENSP00000398136.2:n.451-242C>T | |
| ENST00000524788.1:n.502C>T | ||
| ENST00000528807.1:n.352C>T | ||
| ENST00000533371.5:c.73C>T | ENSP00000437066.1:p.Arg25Trp | |
| ENST00000611494.4:c.802C>T | ENSP00000484546.1:p.Arg268Trp | |
| NM_000391.3:c.802C>T | NP_000382.3:p.Arg268Trp | |
| NM_000391.4:c.802C>T MANE Select | NP_000382.3:p.Arg268Trp |