Revel Score:
ENST00000525803
0.524
ENST00000280362 (MANE Select)
0.762
ENST00000524931
0.762
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.112233178C>G , CM000673.2:g.112233178C>G | GRCh38 |
| NC_000011.9:g.112103901C>G , CM000673.1:g.112103901C>G | GRCh37 |
| NC_000011.8:g.111609111C>G | NCBI36 |
| NG_008743.1:g.11814C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000280362.8:c.259C>G MANE Select | ENSP00000280362.3:p.Pro87Ala | |
| ENST00000280362.7:c.259C>G | ENSP00000280362.3:p.Pro87Ala | |
| ENST00000524931.1:c.55C>G | ENSP00000434688.1:p.Pro19Ala | |
| ENST00000525803.1:c.179C>G | ENSP00000431750.1:p.Ala60Gly | |
| ENST00000527428.5:n.433C>G | ||
| ENST00000527635.1:n.300C>G | ||
| ENST00000528679.5:c.*68C>G | ENSP00000435895.1:n.*68C>G | |
| ENST00000531175.1:n.210C>G | ||
| ENST00000531673.5:c.*68C>G | ENSP00000433469.1:n.*68C>G | |
| NM_000317.2:c.259C>G | NP_000308.1:p.Pro87Ala | |
| XM_011542943.1:c.220C>G | XP_011541245.1:p.Pro74Ala | |
| NM_000317.3:c.259C>G MANE Select | NP_000308.1:p.Pro87Ala |