Revel Score:
ENST00000455537 (MANE Select)
0.918
ENST00000286452
0.918
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57569403C>T , CM000674.2:g.57569403C>T | GRCh38 |
| NC_000012.11:g.57963186C>T , CM000674.1:g.57963186C>T | GRCh37 |
| NC_000012.10:g.56249453C>T | NCBI36 |
| NG_008155.1:g.24340C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000455537.7:c.967C>T MANE Select | ENSP00000408979.2:p.Arg323Trp | |
| ENST00000674619.1:c.967C>T | ENSP00000502270.1:p.Arg323Trp | |
| ENST00000676081.1:n.113C>T | ||
| ENST00000676457.1:c.862C>T | ENSP00000501588.1:p.Arg288Trp | |
| ENST00000286452.5:c.700C>T | ENSP00000286452.5:p.Arg234Trp | |
| ENST00000455537.6:c.967C>T | ENSP00000408979.2:p.Arg323Trp | |
| NM_004984.2:c.967C>T | NP_004975.2:p.Arg323Trp | |
| NM_001354705.1:c.700C>T | NP_001341634.1:p.Arg234Trp | |
| NM_004984.3:c.967C>T | NP_004975.2:p.Arg323Trp | |
| XR_002957324.1:n.1200C>T | ||
| NM_004984.4:c.967C>T MANE Select | NP_004975.2:p.Arg323Trp | |
| NM_001354705.2:c.700C>T | NP_001341634.1:p.Arg234Trp |