Revel Score:
ENST00000371712 (MANE Select)
0.951
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00000369 (NFE)
Exomes Max Group AF
0.00000393 (NFE)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136432563G>A , CM000671.2:g.136432563G>A | GRCh38 |
| NC_000009.11:g.139327015G>A , CM000671.1:g.139327015G>A | GRCh37 |
| NC_000009.10:g.138446836G>A | NCBI36 |
| NG_016126.1:g.12242C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371712.4:c.1303C>T MANE Select | ENSP00000360777.3:p.Arg435Trp | |
| ENST00000676019.1:c.1201C>T | ENSP00000501984.1:p.Arg401Trp | |
| ENST00000371712.3:c.1303C>T | ENSP00000360777.3:p.Arg435Trp | |
| NM_019892.4:c.1303C>T | NP_063945.2:p.Arg435Trp | |
| XM_005266094.2:c.1300C>T | XP_005266151.1:p.Arg434Trp | |
| XR_929828.1:n.1743C>T | ||
| NM_001318502.1:c.1300C>T | NP_001305431.1:p.Arg434Trp | |
| NM_019892.5:c.1303C>T | NP_063945.2:p.Arg435Trp | |
| XM_017014926.1:c.1303C>T | XP_016870415.1:p.Arg435Trp | |
| XR_929828.2:n.1745C>T | ||
| NM_019892.6:c.1303C>T MANE Select | NP_063945.2:p.Arg435Trp | |
| NM_001318502.2:c.1300C>T | NP_001305431.1:p.Arg434Trp |