Revel Score:
ENST00000553106 (MANE Select)
0.861
ENST00000307000
0.861
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102844350A>C , CM000674.2:g.102844350A>C | GRCh38 |
| NC_000012.11:g.103238128A>C , CM000674.1:g.103238128A>C | GRCh37 |
| NC_000012.10:g.101762258A>C | NCBI36 |
| NG_008690.1:g.78253T>G | |
| NG_008690.2:g.119061T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.1051T>G MANE Select | ENSP00000448059.1:p.Phe351Val | |
| ENST00000307000.7:c.1036T>G | ENSP00000303500.2:p.Phe346Val | |
| ENST00000549247.6:n.810T>G | ||
| ENST00000551114.2:n.713T>G | ||
| ENST00000553106.5:c.1051T>G | ENSP00000448059.1:p.Phe351Val | |
| ENST00000635477.1:c.155T>G | ||
| ENST00000635528.1:n.566T>G | ||
| NM_000277.1:c.1051T>G | NP_000268.1:p.Phe351Val | |
| XM_011538422.1:c.994T>G | XP_011536724.1:p.Phe332Val | |
| NM_000277.2:c.1051T>G | NP_000268.1:p.Phe351Val | |
| NM_001354304.1:c.1051T>G | NP_001341233.1:p.Phe351Val | |
| NM_000277.3:c.1051T>G MANE Select | NP_000268.1:p.Phe351Val | |
| NM_001354304.2:c.1051T>G | NP_001341233.1:p.Phe351Val |