Linked Data
ClinVar Variation Id:
13911
dbSNP Id:
rs75996173
ExAC:
10:43609949 G / T
gnomAD v2:
10-43609949-G-T
gnomAD v4:
10-43114501-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43114501G>T , CM000672.2:g.43114501G>T | GRCh38 |
| NC_000010.10:g.43609949G>T , CM000672.1:g.43609949G>T | GRCh37 |
| NC_000010.9:g.42929955G>T | NCBI36 |
| NG_007489.1:g.42433G>T , LRG_518:g.42433G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000615310.5:c.1505G>T | ENSP00000480088.2:p.Cys502Phe | |
| ENST00000683007.1:n.1475G>T | ||
| ENST00000683872.1:n.1466G>T | ||
| ENST00000340058.6:c.1901G>T | ENSP00000344798.4:p.Cys634Phe | |
| ENST00000355710.8:c.1901G>T MANE Select | ENSP00000347942.3:p.Cys634Phe | |
| ENST00000671844.1:c.*495G>T | ENSP00000500541.1:n.*495G>T | |
| ENST00000672389.1:c.*495G>T | ENSP00000500252.1:n.*495G>T | |
| ENST00000340058.5:c.1901G>T | ENSP00000344798.4:p.Cys634Phe | |
| ENST00000355710.7:c.1901G>T | ENSP00000347942.3:p.Cys634Phe | |
| ENST00000498820.5:c.452G>T | ENSP00000419080.1:p.Cys151Phe | |
| ENST00000615310.4:c.1289+3269G>T | ENSP00000480088.1:n.1289+3269G>T | |
| NM_020630.4:c.1901G>T , LRG_518t2:c.1901G>T | NP_065681.1:p.Cys634Phe | |
| NM_020975.4:c.1901G>T , LRG_518t1:c.1901G>T | NP_066124.1:p.Cys634Phe | |
| XM_011540027.1:c.1901G>T | XP_011538329.1:p.Cys634Phe | |
| NM_001355216.1:c.1139G>T | NP_001342145.1:p.Cys380Phe | |
| NM_020630.5:c.1901G>T | NP_065681.1:p.Cys634Phe | |
| NM_020975.5:c.1901G>T | NP_066124.1:p.Cys634Phe | |
| NM_020975.6:c.1901G>T MANE Select | NP_066124.1:p.Cys634Phe | |
| NM_020630.6:c.1901G>T | NP_065681.1:p.Cys634Phe |