Revel Score:
ENST00000305046 (MANE Select)
0.354
ENST00000394887
0.354
ENST00000412614
0.354
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.99318064C>T , CM000666.2:g.99318064C>T | GRCh38 |
| NC_000004.11:g.100239221C>T , CM000666.1:g.100239221C>T | GRCh37 |
| NC_000004.10:g.100458244C>T | NCBI36 |
| NG_011435.1:g.8352G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305046.13:c.241G>A MANE Select | ENSP00000306606.8:p.Val81Met | |
| ENST00000639454.1:c.241G>A | ENSP00000491622.1:p.Val81Met | |
| ENST00000305046.12:c.241G>A | ENSP00000306606.8:p.Val81Met | |
| ENST00000504498.1:n.295G>A | ||
| ENST00000506651.5:c.121G>A | ENSP00000425998.2:p.Val41Met | |
| ENST00000515694.4:n.2336G>A | ||
| ENST00000625860.2:c.121G>A | ENSP00000486614.1:p.Val41Met | |
| ENST00000632775.1:n.804G>A | ||
| NM_000668.5:c.241G>A | NP_000659.2:p.Val81Met | |
| NM_001286650.1:c.121G>A | NP_001273579.1:p.Val41Met | |
| NM_000668.6:c.241G>A MANE Select | NP_000659.2:p.Val81Met | |
| NM_001286650.2:c.121G>A | NP_001273579.1:p.Val41Met |