Revel Score:
ENST00000271588 (MANE Select)
0.256
ENST00000367492
0.256
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186130060C>G , CM000663.2:g.186130060C>G | GRCh38 |
| NC_000001.10:g.186099192C>G , CM000663.1:g.186099192C>G | GRCh37 |
| NC_000001.9:g.184365815C>G | NCBI36 |
| NG_011841.1:g.400510C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.12999C>G MANE Select | ENSP00000271588.4:p.Ser4333Arg | |
| ENST00000271588.8:c.12999C>G | ENSP00000271588.4:p.Ser4333Arg | |
| NM_031935.2:c.12999C>G | NP_114141.2:p.Ser4333Arg | |
| XM_011510037.1:c.12714C>G | XP_011508339.1:p.Ser4238Arg | |
| XM_011510038.1:c.12999C>G | XP_011508340.1:p.Ser4333Arg | |
| XM_011510039.1:c.12999C>G | XP_011508341.1:p.Ser4333Arg | |
| XM_011510038.3:c.12999C>G | XP_011508340.1:p.Ser4333Arg | |
| XM_017002437.1:c.11022C>G | XP_016857926.1:p.Ser3674Arg | |
| NM_031935.3:c.12999C>G MANE Select | NP_114141.2:p.Ser4333Arg |