Revel Score:
ENST00000404648
0.847
ENST00000405164
0.847
ENST00000336098 (MANE Select)
0.847
ENST00000407946
0.847
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.154606768C>A , CM000666.2:g.154606768C>A | GRCh38 |
| NC_000004.11:g.155527920C>A , CM000666.1:g.155527920C>A | GRCh37 |
| NC_000004.10:g.155747370C>A | NCBI36 |
| NG_008834.1:g.10983G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000336098.8:c.1066G>T MANE Select | ENSP00000336829.3:p.Asp356Tyr | |
| ENST00000336098.7:c.1066G>T | ENSP00000336829.3:p.Asp356Tyr | |
| ENST00000404648.7:c.1066G>T | ENSP00000384860.3:p.Asp356Tyr | |
| ENST00000405164.5:c.1090G>T | ENSP00000384101.1:p.Asp364Tyr | |
| ENST00000407946.5:c.1090G>T | ENSP00000384552.1:p.Asp364Tyr | |
| ENST00000465913.1:n.614G>T | ||
| ENST00000492082.5:n.1608G>T | ||
| NM_000509.4:c.1066G>T | NP_000500.2:p.Asp356Tyr | |
| NM_000509.5:c.1066G>T | NP_000500.2:p.Asp356Tyr | |
| NM_021870.2:c.1066G>T | NP_068656.2:p.Asp356Tyr | |
| NM_021870.3:c.1066G>T MANE Select | NP_068656.2:p.Asp356Tyr | |
| NM_000509.6:c.1066G>T | NP_000500.2:p.Asp356Tyr |