Revel Score:
ENST00000320868 (MANE Select)
0.951
ENST00000397797
0.951
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.177116G>T , CM000678.2:g.177116G>T | GRCh38 |
| NC_000016.9:g.227115G>T , CM000678.1:g.227115G>T | GRCh37 |
| NC_000016.8:g.167115G>T | NCBI36 |
| NG_000006.1:g.37979G>T | |
| NG_059186.1:g.5466G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320868.9:c.283G>T MANE Select | ENSP00000322421.5:p.Asp95Tyr | |
| ENST00000397797.1:c.187G>T | ENSP00000380899.1:p.Asp63Tyr | |
| ENST00000472694.1:n.419G>T | ||
| ENST00000487791.1:n.252G>T | ||
| NM_000558.4:c.283G>T | NP_000549.1:p.Asp95Tyr | |
| NM_000558.5:c.283G>T MANE Select | NP_000549.1:p.Asp95Tyr |