Revel Score:
ENST00000367409 (MANE Select)
0.045
ENST00000294732
0.045
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.197142537G>C , CM000663.2:g.197142537G>C | GRCh38 |
| NC_000001.10:g.197111667G>C , CM000663.1:g.197111667G>C | GRCh37 |
| NC_000001.9:g.195378290G>C | NCBI36 |
| NG_015867.1:g.9158C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367409.9:c.1715C>G MANE Select | ENSP00000356379.4:p.Ala572Gly | |
| ENST00000679766.1:n.1932C>G | ||
| ENST00000680265.1:c.1715C>G | ENSP00000505384.1:p.Ala572Gly | |
| ENST00000680710.1:c.1715C>G | ENSP00000506676.1:p.Ala572Gly | |
| ENST00000681879.1:c.1715C>G | ENSP00000505363.1:p.Ala572Gly | |
| ENST00000294732.11:c.1715C>G | ENSP00000294732.7:p.Ala572Gly | |
| ENST00000367409.8:c.1715C>G | ENSP00000356379.4:p.Ala572Gly | |
| ENST00000612785.1:c.561+1154C>G | ENSP00000479244.1:n.561+1154C>G | |
| NM_001206846.1:c.1715C>G | NP_001193775.1:p.Ala572Gly | |
| NM_018136.4:c.1715C>G | NP_060606.3:p.Ala572Gly | |
| NM_018136.5:c.1715C>G MANE Select | NP_060606.3:p.Ala572Gly | |
| NM_001206846.2:c.1715C>G | NP_001193775.1:p.Ala572Gly |