Revel Score:
ENST00000370258
0.902
ENST00000370263 (MANE Select)
0.902
ENST00000539366
0.902
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.63350560G>C , CM000682.2:g.63350560G>C | GRCh38 |
| NC_000020.10:g.61981912G>C , CM000682.1:g.61981912G>C | GRCh37 |
| NC_000020.9:g.61452356G>C | NCBI36 |
| NG_011931.1:g.15784C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370263.9:c.851C>G MANE Select | ENSP00000359285.4:p.Ser284Trp | |
| ENST00000370263.8:c.851C>G | ENSP00000359285.4:p.Ser284Trp | |
| ENST00000463705.5:n.1499C>G | ||
| ENST00000467563.3:n.921C>G | ||
| ENST00000498043.6:c.875C>G | ||
| ENST00000615287.4:c.638C>G | ENSP00000483388.1:p.Ser213Trp | |
| ENST00000627000.1:c.*540C>G | ENSP00000486914.1:n.*540C>G | |
| ENST00000630240.1:n.572C>G | ||
| NM_000744.6:c.851C>G | NP_000735.1:p.Ser284Trp | |
| NM_001256573.1:c.323C>G | NP_001243502.1:p.Ser108Trp | |
| NR_046317.1:n.1107C>G | ||
| XM_011528524.1:c.638C>G | XP_011526826.1:p.Ser213Trp | |
| XM_017027625.2:c.323C>G | XP_016883114.1:p.Ser108Trp | |
| XM_024451822.1:c.323C>G | XP_024307590.1:p.Ser108Trp | |
| NM_001256573.2:c.323C>G | NP_001243502.1:p.Ser108Trp | |
| NR_046317.2:n.1060C>G | ||
| NM_000744.7:c.851C>G MANE Select | NP_000735.1:p.Ser284Trp |