Revel Score:
ENST00000248633 (MANE Select)
0.925
ENST00000428214
0.925
ENST00000545192
0.925
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.92519009C>A , CM000669.2:g.92519009C>A | GRCh38 |
| NC_000007.13:g.92148323C>A , CM000669.1:g.92148323C>A | GRCh37 |
| NC_000007.12:g.91986259C>A | NCBI36 |
| NG_008341.1:g.14523G>T | |
| NG_008341.2:g.14523G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000248633.9:c.343G>T MANE Select | ENSP00000248633.4:p.Asp115Tyr | |
| ENST00000248633.8:c.343G>T | ENSP00000248633.4:p.Asp115Tyr | |
| ENST00000428214.5:c.343G>T | ENSP00000394413.1:p.Asp115Tyr | |
| ENST00000438045.5:c.273+3093G>T | ENSP00000410438.1:n.273+3093G>T | |
| ENST00000484913.5:n.347G>T | ||
| NM_000466.2:c.343G>T | NP_000457.1:p.Asp115Tyr | |
| NM_001282677.1:c.343G>T | NP_001269606.1:p.Asp115Tyr | |
| NM_001282678.1:c.-317G>T | NP_001269607.1:n.-317G>T | |
| XR_242246.3:n.439G>T | ||
| XR_242246.5:n.390G>T | ||
| NM_000466.3:c.343G>T MANE Select | NP_000457.1:p.Asp115Tyr | |
| NM_001282677.2:c.343G>T | NP_001269606.1:p.Asp115Tyr | |
| NM_001282678.2:c.-317G>T | NP_001269607.1:n.-317G>T |