Revel Score:
ENST00000320580 (MANE Select)
0.638
ENST00000533756
0.638
ENST00000527380
0.638
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66211219G>T , CM000673.2:g.66211219G>T | GRCh38 |
| NC_000011.9:g.65978690G>T , CM000673.1:g.65978690G>T | GRCh37 |
| NC_000011.8:g.65735266G>T | NCBI36 |
| NG_033900.1:g.145867G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320580.9:c.620G>T MANE Select | ENSP00000316454.4:p.Gly207Val | |
| ENST00000320580.8:c.620G>T | ENSP00000316454.4:p.Gly207Val | |
| ENST00000527224.1:n.744G>T | ||
| ENST00000527380.1:c.326G>T | ENSP00000432639.1:p.Gly109Val | |
| ENST00000533756.5:c.311G>T | ENSP00000437150.1:p.Gly104Val | |
| NM_018026.3:c.620G>T | NP_060496.2:p.Gly207Val | |
| XM_011545162.1:c.299G>T | XP_011543464.1:p.Gly100Val | |
| XM_011545163.1:c.290G>T | XP_011543465.1:p.Gly97Val | |
| XM_011545164.1:c.281G>T | XP_011543466.1:p.Gly94Val | |
| XM_011545164.2:c.281G>T | XP_011543466.1:p.Gly94Val | |
| XR_001747924.1:n.831G>T | ||
| NM_018026.4:c.620G>T MANE Select | NP_060496.2:p.Gly207Val |