Revel Score:
ENST00000218099 (MANE Select)
0.446
ENST00000394090
0.446
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139561763T>G , CM000685.2:g.139561763T>G | GRCh38 |
| NC_000023.10:g.138643922T>G , CM000685.1:g.138643922T>G | GRCh37 |
| NC_000023.9:g.138471588T>G | NCBI36 |
| NG_007994.1:g.36028T>G , LRG_556:g.36028T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.1078T>G MANE Select | ENSP00000218099.2:p.Phe360Val | |
| ENST00000643157.1:n.1723+22T>G | ||
| ENST00000218099.6:c.1078T>G | ENSP00000218099.2:p.Phe360Val | |
| ENST00000394090.2:c.964T>G | ENSP00000377650.2:p.Phe322Val | |
| NM_000133.3:c.1078T>G , LRG_556t1:c.1078T>G | NP_000124.1:p.Phe360Val | |
| NM_001313913.1:c.964T>G | NP_001300842.1:p.Phe322Val | |
| XM_005262397.3:c.949T>G | XP_005262454.1:p.Phe317Val | |
| XM_005262397.4:c.949T>G | XP_005262454.1:p.Phe317Val | |
| NM_000133.4:c.1078T>G MANE Select | NP_000124.1:p.Phe360Val | |
| NM_001313913.2:c.964T>G | NP_001300842.1:p.Phe322Val |