Revel Score:
ENST00000251595 (MANE Select)
0.672
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.172955T>A , CM000678.2:g.172955T>A | GRCh38 |
| NC_000016.9:g.222954T>A , CM000678.1:g.222954T>A | GRCh37 |
| NC_000016.8:g.162954T>A | NCBI36 |
| NG_000006.1:g.33818T>A | |
| NG_059186.1:g.1305T>A | |
| NG_059271.1:g.5109T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000251595.11:c.43T>A MANE Select | ENSP00000251595.6:p.Trp15Arg | |
| ENST00000251595.10:c.43T>A | ENSP00000251595.6:p.Trp15Arg | |
| ENST00000397806.1:c.-5T>A | ENSP00000380908.1:n.-5T>A | |
| ENST00000482565.1:n.62T>A | ||
| ENST00000484216.1:n.12T>A | ||
| NM_000517.4:c.43T>A | NP_000508.1:p.Trp15Arg | |
| NM_000517.6:c.43T>A MANE Select | NP_000508.1:p.Trp15Arg |