Revel Score:
ENST00000271588 (MANE Select)
0.600
ENST00000367492
0.600
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186003718T>A , CM000663.2:g.186003718T>A | GRCh38 |
| NC_000001.10:g.185972850T>A , CM000663.1:g.185972850T>A | GRCh37 |
| NC_000001.9:g.184239473T>A | NCBI36 |
| NG_011841.1:g.274168T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.4349T>A MANE Select | ENSP00000271588.4:p.Val1450Asp | |
| ENST00000271588.8:c.4349T>A | ENSP00000271588.4:p.Val1450Asp | |
| NM_031935.2:c.4349T>A | NP_114141.2:p.Val1450Asp | |
| XM_011510037.1:c.4349T>A | XP_011508339.1:p.Val1450Asp | |
| XM_011510038.1:c.4349T>A | XP_011508340.1:p.Val1450Asp | |
| XM_011510039.1:c.4349T>A | XP_011508341.1:p.Val1450Asp | |
| XM_011510040.1:c.4349T>A | XP_011508342.1:p.Val1450Asp | |
| XM_011510041.1:c.4349T>A | XP_011508343.1:p.Val1450Asp | |
| XM_011510038.3:c.4349T>A | XP_011508340.1:p.Val1450Asp | |
| XM_011510041.3:c.4349T>A | XP_011508343.1:p.Val1450Asp | |
| XM_017002437.1:c.2372T>A | XP_016857926.1:p.Val791Asp | |
| XM_024450118.1:c.4349T>A | XP_024305886.1:p.Val1450Asp | |
| NM_031935.3:c.4349T>A MANE Select | NP_114141.2:p.Val1450Asp |