Revel Score:
ENST00000167586 (MANE Select)
0.411
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41583782G>A , CM000679.2:g.41583782G>A | GRCh38 |
| NC_000017.10:g.39740034G>A , CM000679.1:g.39740034G>A | GRCh37 |
| NC_000017.9:g.36993560G>A | NCBI36 |
| NG_008624.1:g.8114C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.905C>T MANE Select | ENSP00000167586.6:p.Ala302Val | |
| ENST00000167586.6:c.905C>T | ENSP00000167586.6:p.Ala302Val | |
| ENST00000476662.1:n.355C>T | ||
| NM_000526.4:c.905C>T | NP_000517.2:p.Ala302Val | |
| NM_000526.5:c.905C>T MANE Select | NP_000517.3:p.Ala302Val |