Revel Score:
ENST00000316623 (MANE Select)
0.872
ENST00000389087
0.872
ENST00000544030
0.872
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.48446712A>G , CM000677.2:g.48446712A>G | GRCh38 |
| NC_000015.9:g.48738909A>G , CM000677.1:g.48738909A>G | GRCh37 |
| NC_000015.8:g.46526201A>G | NCBI36 |
| NG_008805.2:g.204077T>C , LRG_778:g.204077T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000559133.6:c.5782T>C | ENSP00000453958.2:p.Cys1928Arg | |
| ENST00000674301.2:c.5782T>C | ENSP00000501333.2:p.Cys1928Arg | |
| ENST00000684448.1:n.4456T>C | ||
| ENST00000316623.10:c.5782T>C MANE Select | ENSP00000325527.5:p.Cys1928Arg | |
| ENST00000674301.1:c.781T>C | ENSP00000501333.1:p.Cys261Arg | |
| ENST00000316623.9:c.5782T>C | ENSP00000325527.5:p.Cys1928Arg | |
| ENST00000537463.6:c.*1545T>C | ENSP00000440294.2:n.*1545T>C | |
| ENST00000559133.5:c.1089T>C | ||
| NM_000138.4:c.5782T>C , LRG_778t1:c.5782T>C | NP_000129.3:p.Cys1928Arg | |
| NM_000138.5:c.5782T>C MANE Select | NP_000129.3:p.Cys1928Arg |