Revel Score:
ENST00000320868 (MANE Select)
0.564
ENST00000397797
0.564
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177332A>C , CM000678.2:g.177332A>C | GRCh38 |
| NC_000016.9:g.227331A>C , CM000678.1:g.227331A>C | GRCh37 |
| NC_000016.8:g.167331A>C | NCBI36 |
| NG_000006.1:g.38195A>C | |
| NG_059186.1:g.5682A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.350A>C MANE Select | ENSP00000322421.5:p.Glu117Ala | |
| ENST00000397797.1:c.254A>C | ENSP00000380899.1:p.Glu85Ala | |
| ENST00000472694.1:n.486A>C | ||
| NM_000558.4:c.350A>C | NP_000549.1:p.Glu117Ala | |
| NM_000558.5:c.350A>C MANE Select | NP_000549.1:p.Glu117Ala |