Revel Score:
ENST00000039007 (MANE Select)
0.938
gnomAD v2:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38401313T>G , CM000685.2:g.38401313T>G | GRCh38 |
| NC_000023.10:g.38260566T>G , CM000685.1:g.38260566T>G | GRCh37 |
| NC_000023.9:g.38145510T>G | NCBI36 |
| NG_008471.1:g.53831T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.425T>G MANE Select | ENSP00000039007.4:p.Val142Gly | |
| ENST00000643344.1:c.*175T>G | ENSP00000496606.1:n.*175T>G | |
| ENST00000039007.4:c.425T>G | ENSP00000039007.4:p.Val142Gly | |
| ENST00000465127.1:c.172-264808T>G | ENSP00000417050.1:n.172-264808T>G | |
| ENST00000488812.1:n.462T>G | ||
| NM_000531.5:c.425T>G | NP_000522.3:p.Val142Gly | |
| XM_017029556.1:c.425T>G | XP_016885045.1:p.Val142Gly | |
| NM_000531.6:c.425T>G MANE Select | NP_000522.3:p.Val142Gly |