Revel Score:
ENST00000375499 (MANE Select)
0.966
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.17024041A>T , CM000663.2:g.17024041A>T | GRCh38 |
| NC_000001.10:g.17350536A>T , CM000663.1:g.17350536A>T | GRCh37 |
| NC_000001.9:g.17223123A>T | NCBI36 |
| NG_012340.1:g.35130T>A , LRG_316:g.35130T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000463045.3:c.403T>A | ENSP00000481376.2:p.Cys135Ser | |
| ENST00000491274.6:c.532T>A | ENSP00000480482.2:p.Cys178Ser | |
| ENST00000375499.8:c.574T>A MANE Select | ENSP00000364649.3:p.Cys192Ser | |
| ENST00000375499.7:c.574T>A | ENSP00000364649.3:p.Cys192Ser | |
| ENST00000485515.5:n.508T>A | ||
| ENST00000491274.5:c.532T>A | ENSP00000480482.1:p.Cys178Ser | |
| NM_003000.2:c.574T>A , LRG_316t1:c.574T>A | NP_002991.2:p.Cys192Ser | |
| NM_003000.3:c.574T>A MANE Select | NP_002991.2:p.Cys192Ser |