Linked Data
ClinVar Variation Id:
313218
dbSNP Id:
rs200360968
ExAC:
14:45650888 C / T
gnomAD v2:
14-45650888-C-T
gnomAD v3:
14-45181685-C-T
gnomAD v4:
14-45181685-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.45181685C>T , CM000676.2:g.45181685C>T | GRCh38 |
| NC_000014.8:g.45650888C>T , CM000676.1:g.45650888C>T | GRCh37 |
| NC_000014.7:g.44720638C>T | NCBI36 |
| NG_007417.1:g.50753C>T , LRG_502:g.50753C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000554809.6:c.2578C>T | ENSP00000450632.2:p.Arg860Cys | |
| ENST00000555484.2:c.144C>T | ||
| ENST00000556250.6:c.4159C>T | ENSP00000452033.2:p.Arg1387Cys | |
| ENST00000557110.2:c.144C>T | ||
| ENST00000696642.1:c.*3177C>T | ENSP00000512775.1:n.*3177C>T | |
| ENST00000696644.1:n.102C>T | ||
| ENST00000696647.1:c.4366C>T | ENSP00000512778.1:p.Arg1456Cys | |
| ENST00000696648.1:c.*2391C>T | ENSP00000512779.1:n.*2391C>T | |
| ENST00000696649.1:c.4210C>T | ENSP00000512780.1:p.Arg1404Cys | |
| ENST00000696650.1:n.4314C>T | ||
| ENST00000696659.1:c.2364C>T | ||
| ENST00000696663.1:c.3297C>T | ||
| ENST00000696664.1:c.3183C>T | ||
| ENST00000696665.1:c.144C>T | ||
| ENST00000696675.1:c.*122C>T | ENSP00000512799.1:n.*122C>T | |
| ENST00000696683.1:c.3183C>T | ||
| ENST00000696684.1:c.3183C>T | ||
| ENST00000696685.1:c.3183C>T | ||
| ENST00000696686.1:n.1103C>T | ||
| ENST00000267430.10:c.4366C>T MANE Select | ENSP00000267430.5:p.Arg1456Cys | |
| ENST00000267430.9:c.4366C>T | ENSP00000267430.5:p.Arg1456Cys | |
| ENST00000542564.6:c.4288C>T | ENSP00000442493.2:p.Arg1430Cys | |
| ENST00000554809.5:c.1163C>T | ||
| ENST00000555013.1:n.199C>T | ||
| ENST00000556250.5:c.2914C>T | ENSP00000452033.1:p.Arg972Cys | |
| NM_001308133.1:c.4288C>T | NP_001295062.1:p.Arg1430Cys | |
| NM_020937.2:c.4366C>T , LRG_502t1:c.4366C>T | NP_065988.1:p.Arg1456Cys | |
| NM_020937.3:c.4366C>T | NP_065988.1:p.Arg1456Cys | |
| XM_011537034.1:c.4366C>T | XP_011535336.1:p.Arg1456Cys | |
| XM_011537035.1:c.4288C>T | XP_011535337.1:p.Arg1430Cys | |
| XM_011537036.1:c.4366C>T | XP_011535338.1:p.Arg1456Cys | |
| XM_011537037.1:c.2380C>T | XP_011535339.1:p.Arg794Cys | |
| XM_011537034.2:c.4366C>T | XP_011535336.1:p.Arg1456Cys | |
| XM_011537035.3:c.4288C>T | XP_011535337.1:p.Arg1430Cys | |
| XM_011537037.3:c.2380C>T | XP_011535339.1:p.Arg794Cys | |
| XM_017021523.1:c.4366C>T | XP_016877012.1:p.Arg1456Cys | |
| XM_017021524.2:c.3403C>T | XP_016877013.1:p.Arg1135Cys | |
| XM_017021525.2:c.3181C>T | XP_016877014.1:p.Arg1061Cys | |
| XM_017021526.2:c.3181C>T | XP_016877015.1:p.Arg1061Cys | |
| XM_017021527.1:c.3181C>T | XP_016877016.1:p.Arg1061Cys | |
| XR_001750470.1:n.4458C>T | ||
| XR_001750471.2:n.4458C>T | ||
| XR_001750472.1:n.4510C>T | ||
| NM_020937.4:c.4366C>T MANE Select | NP_065988.1:p.Arg1456Cys | |
| NM_001308133.2:c.4288C>T | NP_001295062.1:p.Arg1430Cys |