Revel Score:
ENST00000277541
0.904
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136523014C>A , CM000671.2:g.136523014C>A | GRCh38 |
| NC_000009.11:g.139417466C>A , CM000671.1:g.139417466C>A | GRCh37 |
| NC_000009.10:g.138537287C>A | NCBI36 |
| NG_007458.1:g.27773G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000491649.2:n.357G>T | ||
| ENST00000651671.1:c.578G>T MANE Select | ENSP00000498587.1:p.Gly193Val | |
| ENST00000679595.1:c.578G>T | ENSP00000506241.1:p.Gly193Val | |
| ENST00000680133.1:c.578G>T | ENSP00000505319.1:p.Gly193Val | |
| ENST00000680218.1:c.578G>T | ENSP00000505339.1:p.Gly193Val | |
| ENST00000680668.1:c.578G>T | ENSP00000506336.1:p.Gly193Val | |
| ENST00000680924.1:c.578G>T | ENSP00000506031.1:p.Gly193Val | |
| ENST00000681135.1:c.578G>T | ENSP00000506636.1:p.Gly193Val | |
| ENST00000681454.1:c.141-3449G>T | ENSP00000505763.1:n.141-3449G>T | |
| ENST00000277541.6:c.578G>T | ENSP00000277541.6:p.Gly193Val | |
| ENST00000491649.1:n.357G>T | ||
| NM_017617.3:c.578G>T | NP_060087.3:p.Gly193Val | |
| XM_011518717.1:c.44-3449G>T | XP_011517019.1:n.44-3449G>T | |
| NM_017617.5:c.578G>T MANE Select | NP_060087.3:p.Gly193Val | |
| XM_011518717.2:c.20-3449G>T | XP_011517019.2:n.20-3449G>T |