Revel Score:
ENST00000246662 (MANE Select)
0.806
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41571523A>T , CM000679.2:g.41571523A>T | GRCh38 |
| NC_000017.10:g.39727775A>T , CM000679.1:g.39727775A>T | GRCh37 |
| NC_000017.9:g.36981301A>T | NCBI36 |
| NG_008300.1:g.5536T>A | |
| NG_008300.2:g.5536T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000246662.9:c.470T>A MANE Select | ENSP00000246662.4:p.Met157Lys | |
| ENST00000246662.8:c.470T>A | ENSP00000246662.4:p.Met157Lys | |
| ENST00000588431.1:c.-189-41T>A | ENSP00000467932.1:n.-189-41T>A | |
| NM_000226.3:c.470T>A | NP_000217.2:p.Met157Lys | |
| NM_000226.4:c.470T>A MANE Select | NP_000217.2:p.Met157Lys |