Revel Score:
ENST00000316623 (MANE Select)
0.721
ENST00000389087
0.721
ENST00000544030
0.721
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48446710A>C , CM000677.2:g.48446710A>C | GRCh38 |
| NC_000015.9:g.48738907A>C , CM000677.1:g.48738907A>C | GRCh37 |
| NC_000015.8:g.46526199A>C | NCBI36 |
| NG_008805.2:g.204079T>G , LRG_778:g.204079T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.5784T>G | ENSP00000453958.2:p.Cys1928Trp | |
| ENST00000674301.2:c.5784T>G | ENSP00000501333.2:p.Cys1928Trp | |
| ENST00000684448.1:n.4458T>G | ||
| ENST00000316623.10:c.5784T>G MANE Select | ENSP00000325527.5:p.Cys1928Trp | |
| ENST00000674301.1:c.783T>G | ENSP00000501333.1:p.Cys261Trp | |
| ENST00000316623.9:c.5784T>G | ENSP00000325527.5:p.Cys1928Trp | |
| ENST00000537463.6:c.*1547T>G | ENSP00000440294.2:n.*1547T>G | |
| ENST00000559133.5:c.1091T>G | ||
| NM_000138.4:c.5784T>G , LRG_778t1:c.5784T>G | NP_000129.3:p.Cys1928Trp | |
| NM_000138.5:c.5784T>G MANE Select | NP_000129.3:p.Cys1928Trp |