Revel Score:
ENST00000553106 (MANE Select)
0.944
ENST00000307000
0.944
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102866603A>C , CM000674.2:g.102866603A>C | GRCh38 |
| NC_000012.11:g.103260381A>C , CM000674.1:g.103260381A>C | GRCh37 |
| NC_000012.10:g.101784511A>C | NCBI36 |
| NG_008690.1:g.56000T>G | |
| NG_008690.2:g.96808T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.502T>G MANE Select | ENSP00000448059.1:p.Tyr168Asp | |
| ENST00000307000.7:c.487T>G | ENSP00000303500.2:p.Tyr163Asp | |
| ENST00000549111.5:n.598T>G | ||
| ENST00000551988.5:n.530+10859T>G | ||
| ENST00000553106.5:c.502T>G | ENSP00000448059.1:p.Tyr168Asp | |
| NM_000277.1:c.502T>G | NP_000268.1:p.Tyr168Asp | |
| XM_011538422.1:c.502T>G | XP_011536724.1:p.Tyr168Asp | |
| NM_000277.2:c.502T>G | NP_000268.1:p.Tyr168Asp | |
| NM_001354304.1:c.502T>G | NP_001341233.1:p.Tyr168Asp | |
| XM_017019370.2:c.502T>G | XP_016874859.1:p.Tyr168Asp | |
| NM_000277.3:c.502T>G MANE Select | NP_000268.1:p.Tyr168Asp | |
| NM_001354304.2:c.502T>G | NP_001341233.1:p.Tyr168Asp |