Revel Score:
ENST00000271588 (MANE Select)
0.727
ENST00000367492
0.727
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186130050C>G , CM000663.2:g.186130050C>G | GRCh38 |
| NC_000001.10:g.186099182C>G , CM000663.1:g.186099182C>G | GRCh37 |
| NC_000001.9:g.184365805C>G | NCBI36 |
| NG_011841.1:g.400500C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271588.9:c.12989C>G MANE Select | ENSP00000271588.4:p.Ala4330Gly | |
| ENST00000271588.8:c.12989C>G | ENSP00000271588.4:p.Ala4330Gly | |
| NM_031935.2:c.12989C>G | NP_114141.2:p.Ala4330Gly | |
| XM_011510037.1:c.12704C>G | XP_011508339.1:p.Ala4235Gly | |
| XM_011510038.1:c.12989C>G | XP_011508340.1:p.Ala4330Gly | |
| XM_011510039.1:c.12989C>G | XP_011508341.1:p.Ala4330Gly | |
| XM_011510038.3:c.12989C>G | XP_011508340.1:p.Ala4330Gly | |
| XM_017002437.1:c.11012C>G | XP_016857926.1:p.Ala3671Gly | |
| NM_031935.3:c.12989C>G MANE Select | NP_114141.2:p.Ala4330Gly |