Revel Score:
ENST00000263774 (MANE Select)
0.745
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47582139A>T , CM000673.2:g.47582139A>T | GRCh38 |
| NC_000011.9:g.47603691A>T , CM000673.1:g.47603691A>T | GRCh37 |
| NC_000011.8:g.47560267A>T | NCBI36 |
| NG_011946.1:g.8130A>T | |
| NG_011946.2:g.8130A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263774.9:c.433A>T MANE Select | ENSP00000263774.4:p.Thr145Ser | |
| ENST00000531351.2:n.1493A>T | ||
| ENST00000677462.1:n.2907A>T | ||
| ENST00000678975.1:n.2690A>T | ||
| ENST00000263774.8:c.433A>T | ENSP00000263774.4:p.Thr145Ser | |
| ENST00000524568.1:n.536A>T | ||
| ENST00000525212.1:n.88A>T | ||
| ENST00000525378.5:n.371A>T | ||
| ENST00000533507.5:n.1327A>T | ||
| NM_004551.2:c.433A>T | NP_004542.1:p.Thr145Ser | |
| NM_004551.3:c.433A>T MANE Select | NP_004542.1:p.Thr145Ser |