Revel Score:
ENST00000380252
0.500
ENST00000380259
0.500
ENST00000336906 (MANE Select)
0.500
ENST00000380247
0.500
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5253364G>C , CM000673.2:g.5253364G>C | GRCh38 |
| NC_000011.9:g.5274594G>C , CM000673.1:g.5274594G>C | GRCh37 |
| NC_000011.8:g.5231170G>C | NCBI36 |
| NG_000007.3:g.44252C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336906.6:c.357C>G MANE Select | ENSP00000338082.4:p.Phe119Leu | |
| ENST00000380252.6:c.192C>G | ENSP00000369602.2:p.Phe64Leu | |
| ENST00000642908.1:c.315+928C>G | ENSP00000495346.1:n.315+928C>G | |
| ENST00000647543.1:c.357C>G | ENSP00000496470.1:p.Phe119Leu | |
| ENST00000336906.4:c.357C>G | ENSP00000338082.4:p.Phe119Leu | |
| ENST00000380252.5:c.327C>G | ENSP00000369602.1:p.Phe109Leu | |
| ENST00000380259.6:c.357C>G | ENSP00000369609.2:p.Phe119Leu | |
| ENST00000620888.4:c.315+928C>G | ENSP00000479637.1:n.315+928C>G | |
| NM_000184.2:c.357C>G | NP_000175.1:p.Phe119Leu | |
| NM_000184.3:c.357C>G MANE Select | NP_000175.1:p.Phe119Leu |