Revel Score:
ENST00000263967 (MANE Select)
0.881
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.179218286C>A , CM000665.2:g.179218286C>A | GRCh38 |
| NC_000003.11:g.178936074C>A , CM000665.1:g.178936074C>A | GRCh37 |
| NC_000003.10:g.180418768C>A | NCBI36 |
| NG_012113.2:g.74764C>A , LRG_310:g.74764C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263967.4:c.1616C>A MANE Select | ENSP00000263967.3:p.Pro539His | |
| ENST00000462255.2:n.78C>A | ||
| ENST00000643187.1:c.1616C>A | ENSP00000493507.1:p.Pro539His | |
| ENST00000674534.1:n.1370C>A | ||
| ENST00000674622.1:c.119C>A | ENSP00000502417.1:p.Pro40His | |
| ENST00000675467.1:n.4423C>A | ||
| ENST00000675786.1:c.*183C>A | ENSP00000502323.1:n.*183C>A | |
| ENST00000263967.3:c.1616C>A | ENSP00000263967.3:p.Pro539His | |
| NM_006218.2:c.1616C>A , LRG_310t1:c.1616C>A | NP_006209.2:p.Pro539His | |
| XM_006713658.2:c.1616C>A | XP_006713721.1:p.Pro539His | |
| XM_011512894.1:c.1616C>A | XP_011511196.1:p.Pro539His | |
| NM_006218.3:c.1616C>A | NP_006209.2:p.Pro539His | |
| XM_006713658.4:c.1616C>A | XP_006713721.1:p.Pro539His | |
| XM_011512894.2:c.1616C>A | XP_011511196.1:p.Pro539His | |
| NM_006218.4:c.1616C>A MANE Select | NP_006209.2:p.Pro539His |