Linked Data
dbSNP Id:
rs41513147
ExAC:
2:202074200 C / A
gnomAD v2:
2-202074200-C-A
gnomAD v4:
2-201209477-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.201209477C>A , CM000664.2:g.201209477C>A | GRCh38 |
| NC_000002.11:g.202074200C>A , CM000664.1:g.202074200C>A | GRCh37 |
| NC_000002.10:g.201782445C>A | NCBI36 |
| NG_007265.1:g.31346C>A , LRG_33:g.31346C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313728.12:c.1129C>A | ENSP00000314599.7:p.Pro377Thr | |
| ENST00000346817.10:c.1201C>A | ENSP00000237865.7:p.Pro401Thr | |
| ENST00000438843.6:c.*787C>A | ENSP00000401914.1:n.*787C>A | |
| ENST00000492363.6:c.*416C>A | ENSP00000512459.1:n.*416C>A | |
| ENST00000696199.1:c.721+5711C>A | ENSP00000512481.1:n.721+5711C>A | |
| ENST00000286186.11:c.1330C>A MANE Select | ENSP00000286186.6:p.Pro444Thr | |
| ENST00000272879.9:c.1330C>A | ENSP00000272879.5:p.Pro444Thr | |
| ENST00000286186.10:c.1330C>A | ENSP00000286186.6:p.Pro444Thr | |
| ENST00000313728.11:c.1129C>A | ENSP00000314599.7:p.Pro377Thr | |
| ENST00000346817.9:c.1201C>A | ENSP00000237865.7:p.Pro401Thr | |
| ENST00000360132.7:c.*416C>A | ENSP00000353250.3:n.*416C>A | |
| ENST00000448480.1:c.1201C>A | ENSP00000396835.1:p.Pro401Thr | |
| ENST00000492363.5:n.1238C>A | ||
| NM_001206524.1:c.1129C>A | NP_001193453.1:p.Pro377Thr | |
| NM_001206542.1:c.1201C>A | NP_001193471.1:p.Pro401Thr | |
| NM_001230.4:c.1201C>A | NP_001221.2:p.Pro401Thr | |
| NM_032974.4:c.1330C>A | NP_116756.2:p.Pro444Thr | |
| NM_032976.3:c.*416C>A | NP_116758.1:n.*416C>A | |
| NM_032977.3:c.1330C>A , LRG_33t1:c.1330C>A | NP_116759.2:p.Pro444Thr | |
| XM_005246907.2:c.1327C>A | XP_005246964.1:p.Pro443Thr | |
| XM_006712796.2:c.580C>A | XP_006712859.1:p.Pro194Thr | |
| XM_006712796.3:c.580C>A | XP_006712859.1:p.Pro194Thr | |
| NM_001206524.2:c.1129C>A | NP_001193453.1:p.Pro377Thr | |
| NM_001206542.2:c.1201C>A | NP_001193471.1:p.Pro401Thr | |
| NM_001230.5:c.1201C>A | NP_001221.2:p.Pro401Thr | |
| NM_032974.5:c.1330C>A | NP_116756.2:p.Pro444Thr | |
| NM_032977.4:c.1330C>A MANE Select | NP_116759.2:p.Pro444Thr | |
| NM_032976.4:c.*416C>A | NP_116758.1:n.*416C>A |