Revel Score:
ENST00000271588 (MANE Select)
0.336
ENST00000367492
0.336
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186003718T>C , CM000663.2:g.186003718T>C | GRCh38 |
| NC_000001.10:g.185972850T>C , CM000663.1:g.185972850T>C | GRCh37 |
| NC_000001.9:g.184239473T>C | NCBI36 |
| NG_011841.1:g.274168T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.4349T>C MANE Select | ENSP00000271588.4:p.Val1450Ala | |
| ENST00000271588.8:c.4349T>C | ENSP00000271588.4:p.Val1450Ala | |
| NM_031935.2:c.4349T>C | NP_114141.2:p.Val1450Ala | |
| XM_011510037.1:c.4349T>C | XP_011508339.1:p.Val1450Ala | |
| XM_011510038.1:c.4349T>C | XP_011508340.1:p.Val1450Ala | |
| XM_011510039.1:c.4349T>C | XP_011508341.1:p.Val1450Ala | |
| XM_011510040.1:c.4349T>C | XP_011508342.1:p.Val1450Ala | |
| XM_011510041.1:c.4349T>C | XP_011508343.1:p.Val1450Ala | |
| XM_011510038.3:c.4349T>C | XP_011508340.1:p.Val1450Ala | |
| XM_011510041.3:c.4349T>C | XP_011508343.1:p.Val1450Ala | |
| XM_017002437.1:c.2372T>C | XP_016857926.1:p.Val791Ala | |
| XM_024450118.1:c.4349T>C | XP_024305886.1:p.Val1450Ala | |
| NM_031935.3:c.4349T>C MANE Select | NP_114141.2:p.Val1450Ala |