Revel Score:
ENST00000237014 (MANE Select)
0.805
ENST00000432547
0.805
ENST00000541025
0.805
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31592983T>A , CM000680.2:g.31592983T>A | GRCh38 |
| NC_000018.9:g.29172946T>A , CM000680.1:g.29172946T>A | GRCh37 |
| NC_000018.8:g.27426944T>A | NCBI36 |
| NG_009490.1:g.6217T>A , LRG_416:g.6217T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000237014.8:c.157T>A MANE Select | ENSP00000237014.4:p.Phe53Ile | |
| ENST00000610404.5:c.61T>A | ENSP00000477599.2:p.Phe21Ile | |
| ENST00000649620.1:c.157T>A | ENSP00000497927.1:p.Phe53Ile | |
| ENST00000237014.7:c.157T>A | ENSP00000237014.3:p.Phe53Ile | |
| ENST00000432547.7:n.183T>A | ||
| ENST00000541025.2:n.183T>A | ||
| ENST00000610404.4:c.157T>A | ENSP00000477599.1:p.Phe53Ile | |
| ENST00000613781.1:c.157T>A | ENSP00000479174.1:p.Phe53Ile | |
| NM_000371.3:c.157T>A , LRG_416t1:c.157T>A | NP_000362.1:p.Phe53Ile | |
| NM_000371.4:c.157T>A MANE Select | NP_000362.1:p.Phe53Ile |