Revel Score:
ENST00000391911
0.797
ENST00000356082 (MANE Select)
0.797
ENST00000367030
0.797
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.209629743A>T , CM000663.2:g.209629743A>T | GRCh38 |
| NC_000001.10:g.209803088A>T , CM000663.1:g.209803088A>T | GRCh37 |
| NC_000001.9:g.207869711A>T | NCBI36 |
| NG_007116.1:g.27733T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356082.9:c.1126T>A MANE Select | ENSP00000348384.3:p.Cys376Ser | |
| ENST00000356082.8:c.1126T>A | ENSP00000348384.3:p.Cys376Ser | |
| ENST00000367030.7:c.1126T>A | ENSP00000355997.3:p.Cys376Ser | |
| ENST00000391911.5:c.1126T>A | ENSP00000375778.1:p.Cys376Ser | |
| NM_000228.2:c.1126T>A | NP_000219.2:p.Cys376Ser | |
| NM_001017402.1:c.1126T>A | NP_001017402.1:p.Cys376Ser | |
| NM_001127641.1:c.1126T>A | NP_001121113.1:p.Cys376Ser | |
| XM_005273124.3:c.1126T>A | XP_005273181.1:p.Cys376Ser | |
| XM_005273124.4:c.1126T>A | XP_005273181.1:p.Cys376Ser | |
| XM_017001272.2:c.934T>A | XP_016856761.1:p.Cys312Ser | |
| NM_000228.3:c.1126T>A MANE Select | NP_000219.2:p.Cys376Ser | |
| NM_001017402.2:c.1126T>A | NP_001017402.1:p.Cys376Ser |