Revel Score:
ENST00000246515 (MANE Select)
0.564
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.142742343A>T , CM000670.2:g.142742343A>T | GRCh38 |
| NC_000008.10:g.143823761A>T , CM000670.1:g.143823761A>T | GRCh37 |
| NC_000008.9:g.143820763A>T | NCBI36 |
| NG_011494.1:g.5069T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000246515.2:c.43T>A MANE Select | ENSP00000246515.1:p.Trp15Arg | |
| ENST00000246515.1:c.43T>A | ENSP00000246515.1:p.Trp15Arg | |
| NM_020427.2:c.43T>A | NP_065160.1:p.Trp15Arg | |
| NM_020427.3:c.43T>A MANE Select | NP_065160.1:p.Trp15Arg |