Revel Score:
ENST00000350375 (MANE Select)
0.932
ENST00000344265
0.932
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.87262140T>G , CM000665.2:g.87262140T>G | GRCh38 |
| NC_000003.11:g.87311290T>G , CM000665.1:g.87311290T>G | GRCh37 |
| NC_000003.10:g.87393980T>G | NCBI36 |
| NG_008225.2:g.19448A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000344265.8:c.613A>C | ENSP00000342931.3:p.Ser205Arg | |
| ENST00000350375.7:c.535A>C MANE Select | ENSP00000263781.2:p.Ser179Arg | |
| ENST00000344265.7:c.613A>C | ENSP00000342931.3:p.Ser205Arg | |
| ENST00000350375.6:c.535A>C | ENSP00000263781.2:p.Ser179Arg | |
| ENST00000560656.1:c.440-2036A>C | ENSP00000452610.1:n.440-2036A>C | |
| ENST00000561167.5:c.310A>C | ENSP00000454072.1:p.Ser104Arg | |
| NM_000306.3:c.535A>C | NP_000297.1:p.Ser179Arg | |
| NM_001122757.2:c.613A>C | NP_001116229.1:p.Ser205Arg | |
| NM_000306.4:c.535A>C MANE Select | NP_000297.1:p.Ser179Arg | |
| NM_001122757.3:c.613A>C | NP_001116229.1:p.Ser205Arg |