Revel Score:
ENST00000039007 (MANE Select)
0.967
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38401381G>T , CM000685.2:g.38401381G>T | GRCh38 |
| NC_000023.10:g.38260634G>T , CM000685.1:g.38260634G>T | GRCh37 |
| NC_000023.9:g.38145578G>T | NCBI36 |
| NG_008471.1:g.53899G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.493G>T MANE Select | ENSP00000039007.4:p.Asp165Tyr | |
| ENST00000643344.1:c.*243G>T | ENSP00000496606.1:n.*243G>T | |
| ENST00000039007.4:c.493G>T | ENSP00000039007.4:p.Asp165Tyr | |
| ENST00000465127.1:c.172-264740G>T | ENSP00000417050.1:n.172-264740G>T | |
| ENST00000488812.1:n.530G>T | ||
| NM_000531.5:c.493G>T | NP_000522.3:p.Asp165Tyr | |
| XM_017029556.1:c.493G>T | XP_016885045.1:p.Asp165Tyr | |
| NM_000531.6:c.493G>T MANE Select | NP_000522.3:p.Asp165Tyr |