Linked Data
ClinVar Variation Id:
477327
ClinVar RCV Id:
RCV000549713
RCV001013214
RCV001107245
RCV001107247
RCV001107244
RCV001107246
RCV002491103
dbSNP Id:
rs745418960
ExAC:
10:43609042 C / T
gnomAD v2:
10-43609042-C-T
gnomAD v3:
10-43113594-C-T
gnomAD v4:
10-43113594-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.43113594C>T , CM000672.2:g.43113594C>T | GRCh38 |
| NC_000010.10:g.43609042C>T , CM000672.1:g.43609042C>T | GRCh37 |
| NC_000010.9:g.42929048C>T | NCBI36 |
| NG_007489.1:g.41526C>T , LRG_518:g.41526C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000615310.5:c.1402C>T | ENSP00000480088.2:p.Arg468Trp | |
| ENST00000683007.1:n.1372C>T | ||
| ENST00000683872.1:n.559C>T | ||
| ENST00000340058.6:c.1798C>T | ENSP00000344798.4:p.Arg600Trp | |
| ENST00000355710.8:c.1798C>T MANE Select | ENSP00000347942.3:p.Arg600Trp | |
| ENST00000671844.1:c.*392C>T | ENSP00000500541.1:n.*392C>T | |
| ENST00000672389.1:c.*392C>T | ENSP00000500252.1:n.*392C>T | |
| ENST00000340058.5:c.1798C>T | ENSP00000344798.4:p.Arg600Trp | |
| ENST00000355710.7:c.1798C>T | ENSP00000347942.3:p.Arg600Trp | |
| ENST00000498820.5:c.349C>T | ENSP00000419080.1:p.Arg117Trp | |
| ENST00000615310.4:c.1289+2362C>T | ENSP00000480088.1:n.1289+2362C>T | |
| NM_020630.4:c.1798C>T , LRG_518t2:c.1798C>T | NP_065681.1:p.Arg600Trp | |
| NM_020975.4:c.1798C>T , LRG_518t1:c.1798C>T | NP_066124.1:p.Arg600Trp | |
| XM_011540027.1:c.1798C>T | XP_011538329.1:p.Arg600Trp | |
| NM_001355216.1:c.1036C>T | NP_001342145.1:p.Arg346Trp | |
| NM_020630.5:c.1798C>T | NP_065681.1:p.Arg600Trp | |
| NM_020975.5:c.1798C>T | NP_066124.1:p.Arg600Trp | |
| NM_020975.6:c.1798C>T MANE Select | NP_066124.1:p.Arg600Trp | |
| NM_020630.6:c.1798C>T | NP_065681.1:p.Arg600Trp |