Revel Score:
ENST00000389857 (MANE Select)
0.083
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91338150G>C , CM000676.2:g.91338150G>C | GRCh38 |
| NC_000014.8:g.91804494G>C , CM000676.1:g.91804494G>C | GRCh37 |
| NC_000014.7:g.90874247G>C | NCBI36 |
| NG_033118.1:g.84695C>G | |
| NG_033118.2:g.84695C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.905C>G MANE Select | ENSP00000374507.6:p.Ala302Gly | |
| ENST00000389857.10:c.905C>G | ENSP00000374507.6:p.Ala302Gly | |
| ENST00000554051.1:n.382C>G | ||
| NM_001080414.3:c.905C>G | NP_001073883.2:p.Ala302Gly | |
| XM_005267691.3:c.905C>G | XP_005267748.1:p.Ala302Gly | |
| XM_011536796.1:c.797C>G | XP_011535098.1:p.Ala266Gly | |
| XR_429316.2:n.1033C>G | ||
| XR_943459.1:n.1033C>G | ||
| XM_005267691.5:c.905C>G | XP_005267748.1:p.Ala302Gly | |
| XM_011536796.2:c.797C>G | XP_011535098.1:p.Ala266Gly | |
| XM_017021335.2:c.905C>G | XP_016876824.1:p.Ala302Gly | |
| XM_017021337.2:c.905C>G | XP_016876826.1:p.Ala302Gly | |
| XR_429316.4:n.1031C>G | ||
| NM_001080414.4:c.905C>G MANE Select | NP_001073883.2:p.Ala302Gly |