Revel Score:
ENST00000039007 (MANE Select)
0.914
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38401379C>T , CM000685.2:g.38401379C>T | GRCh38 |
| NC_000023.10:g.38260632C>T , CM000685.1:g.38260632C>T | GRCh37 |
| NC_000023.9:g.38145576C>T | NCBI36 |
| NG_008471.1:g.53897C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.491C>T MANE Select | ENSP00000039007.4:p.Ser164Leu | |
| ENST00000643344.1:c.*241C>T | ENSP00000496606.1:n.*241C>T | |
| ENST00000039007.4:c.491C>T | ENSP00000039007.4:p.Ser164Leu | |
| ENST00000465127.1:c.172-264742C>T | ENSP00000417050.1:n.172-264742C>T | |
| ENST00000488812.1:n.528C>T | ||
| NM_000531.5:c.491C>T | NP_000522.3:p.Ser164Leu | |
| XM_017029556.1:c.491C>T | XP_016885045.1:p.Ser164Leu | |
| NM_000531.6:c.491C>T MANE Select | NP_000522.3:p.Ser164Leu |