Revel Score:
ENST00000366684 (MANE Select)
0.963
ENST00000366682
0.963
ENST00000342787
0.963
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.229432567C>A , CM000663.2:g.229432567C>A | GRCh38 |
| NC_000001.10:g.229568314C>A , CM000663.1:g.229568314C>A | GRCh37 |
| NC_000001.9:g.227634937C>A | NCBI36 |
| NG_006672.1:g.6530G>T , LRG_429:g.6530G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366683.4:c.443G>T | ENSP00000355644.4:p.Gly148Val | |
| ENST00000684723.1:c.308G>T | ENSP00000508084.1:p.Gly103Val | |
| ENST00000366683.3:c.443G>T | ENSP00000355644.3:p.Gly148Val | |
| ENST00000366684.7:c.443G>T MANE Select | ENSP00000355645.3:p.Gly148Val | |
| NM_001100.3:c.443G>T , LRG_429t1:c.443G>T | NP_001091.1:p.Gly148Val | |
| NM_001100.4:c.443G>T MANE Select | NP_001091.1:p.Gly148Val |