Revel Score:
ENST00000366560 (MANE Select)
0.939
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.241502525G>T , CM000663.2:g.241502525G>T | GRCh38 |
| NC_000001.10:g.241665825G>T , CM000663.1:g.241665825G>T | GRCh37 |
| NC_000001.9:g.239732448G>T | NCBI36 |
| NG_012338.1:g.22230C>A , LRG_504:g.22230C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000493477.2:n.1657C>A | ||
| ENST00000682162.1:c.1183C>A | ENSP00000508203.1:n.1183C>A | |
| ENST00000682567.1:n.2702C>A | ||
| ENST00000683521.1:c.1154C>A | ENSP00000506864.1:p.Ala385Asp | |
| ENST00000684161.1:n.2369C>A | ||
| ENST00000684483.1:c.*550C>A | ENSP00000507894.1:n.*550C>A | |
| ENST00000366560.4:c.1154C>A MANE Select | ENSP00000355518.4:p.Ala385Asp | |
| ENST00000366560.3:c.1154C>A | ENSP00000355518.3:p.Ala385Asp | |
| NM_000143.3:c.1154C>A , LRG_504t1:c.1154C>A | NP_000134.2:p.Ala385Asp | |
| XM_011544132.1:c.926C>A | XP_011542434.1:p.Ala309Asp | |
| XM_011544132.2:c.926C>A | XP_011542434.1:p.Ala309Asp | |
| NM_000143.4:c.1154C>A MANE Select | NP_000134.2:p.Ala385Asp |