Revel Score:
ENST00000335295 (MANE Select)
0.884
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225620G>A , CM000673.2:g.5225620G>A | GRCh38 |
| NC_000011.9:g.5246850G>A , CM000673.1:g.5246850G>A | GRCh37 |
| NC_000011.8:g.5203426G>A | NCBI36 |
| NG_000007.3:g.71996C>T | |
| NG_059281.1:g.6452C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.422C>T | ENSP00000494175.1:p.Ala141Val | |
| ENST00000335295.4:c.422C>T MANE Select | ENSP00000333994.3:p.Ala141Val | |
| ENST00000633227.1:c.*238C>T | ENSP00000488004.1:n.*238C>T | |
| NM_000518.4:c.422C>T | NP_000509.1:p.Ala141Val | |
| NM_000518.5:c.422C>T MANE Select | NP_000509.1:p.Ala141Val |