Revel Score:
ENST00000413590
0.076
ENST00000337432 (MANE Select)
0.046
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58732524A>T , CM000679.2:g.58732524A>T | GRCh38 |
| NC_000017.10:g.56809885A>T , CM000679.1:g.56809885A>T | GRCh37 |
| NC_000017.9:g.54164884A>T | NCBI36 |
| NG_023199.1:g.44923A>T , LRG_314:g.44923A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.655A>T | ENSP00000464056.2:p.Thr219Ser | |
| ENST00000697680.1:c.*1970A>T | ENSP00000513392.1:n.*1970A>T | |
| ENST00000697681.1:c.*2167A>T | ENSP00000513393.1:n.*2167A>T | |
| ENST00000697683.1:c.*1942A>T | ENSP00000513395.1:n.*1942A>T | |
| ENST00000697685.1:c.*1703A>T | ENSP00000513396.1:n.*1703A>T | |
| ENST00000697686.1:c.777A>T | ENSP00000513397.1:p.Ala259= | |
| ENST00000697689.1:c.*1441-1594A>T | ENSP00000513398.1:n.*1441-1594A>T | |
| ENST00000697690.1:c.905-1594A>T | ENSP00000513399.1:n.905-1594A>T | |
| ENST00000697691.1:c.*978A>T | ENSP00000513400.1:n.*978A>T | |
| ENST00000697692.1:c.*1018A>T | ENSP00000513401.1:n.*1018A>T | |
| ENST00000697694.1:c.655A>T | ENSP00000513402.1:p.Thr219Ser | |
| ENST00000697695.1:n.1613A>T | ||
| ENST00000337432.9:c.1006A>T MANE Select | ENSP00000336701.4:p.Thr336Ser | |
| ENST00000337432.8:c.1006A>T | ENSP00000336701.4:p.Thr336Ser | |
| ENST00000413590.5:c.647A>T | ||
| ENST00000461706.1:n.193A>T | ||
| ENST00000475762.5:c.*1642A>T | ENSP00000432421.1:n.*1642A>T | |
| ENST00000482007.5:c.*434A>T | ENSP00000433332.1:n.*434A>T | |
| ENST00000487525.5:c.*582A>T | ENSP00000431637.1:n.*582A>T | |
| ENST00000578151.1:n.240-1594A>T | ||
| ENST00000581221.5:n.521A>T | ||
| ENST00000583539.5:c.1006A>T | ENSP00000463121.1:p.Thr336Ser | |
| ENST00000584804.1:c.240A>T | ENSP00000463658.1:p.Ala80= | |
| NM_058216.2:c.1006A>T | NP_478123.1:p.Thr336Ser | |
| NR_103872.1:n.910A>T | ||
| XM_006722001.2:c.1009A>T | XP_006722064.1:p.Thr337Ser | |
| XM_006722002.2:c.945A>T | XP_006722065.1:p.Ala315= | |
| XM_006722004.2:c.658A>T | XP_006722067.1:p.Thr220Ser | |
| XM_006722005.2:c.658A>T | XP_006722068.1:p.Thr220Ser | |
| XM_011525092.1:c.658A>T | XP_011523394.1:p.Thr220Ser | |
| XM_011525093.1:c.658A>T | XP_011523395.1:p.Thr220Ser | |
| XM_011525094.1:c.658A>T | XP_011523396.1:p.Thr220Ser | |
| XR_934513.1:n.1224A>T | ||
| XR_934514.1:n.1227A>T | ||
| XR_934886.1:n.149+5547T>A | ||
| XM_006722001.4:c.1009A>T | XP_006722064.1:p.Thr337Ser | |
| XM_006722002.4:c.945A>T | XP_006722065.1:p.Ala315= | |
| XM_006722004.3:c.658A>T | XP_006722067.1:p.Thr220Ser | |
| XM_006722005.3:c.658A>T | XP_006722068.1:p.Thr220Ser | |
| XM_011525092.2:c.658A>T | XP_011523394.1:p.Thr220Ser | |
| XM_011525093.2:c.658A>T | XP_011523395.1:p.Thr220Ser | |
| XM_011525094.2:c.658A>T | XP_011523396.1:p.Thr220Ser | |
| XM_017024914.1:c.655A>T | XP_016880403.1:p.Thr219Ser | |
| XM_017024915.1:c.655A>T | XP_016880404.1:p.Thr219Ser | |
| XM_017024916.1:c.655A>T | XP_016880405.1:p.Thr219Ser | |
| XM_017024917.1:c.655A>T | XP_016880406.1:p.Thr219Ser | |
| XM_017024918.2:c.655A>T | XP_016880407.1:p.Thr219Ser | |
| XM_017024919.1:c.594A>T | XP_016880408.1:p.Ala198= | |
| XR_934513.3:n.1655A>T | ||
| XR_934514.3:n.1658A>T | ||
| XR_934886.2:n.149+5547T>A | ||
| NM_058216.3:c.1006A>T MANE Select | NP_478123.1:p.Thr336Ser | |
| NR_103872.2:n.881A>T |