Revel Score:
ENST00000553106 (MANE Select)
0.584
ENST00000307000
0.584
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102855292T>C , CM000674.2:g.102855292T>C | GRCh38 |
| NC_000012.11:g.103249070T>C , CM000674.1:g.103249070T>C | GRCh37 |
| NC_000012.10:g.101773200T>C | NCBI36 |
| NG_008690.1:g.67311A>G | |
| NG_008690.2:g.108119A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.550A>G MANE Select | ENSP00000448059.1:p.Lys184Glu | |
| ENST00000307000.7:c.535A>G | ENSP00000303500.2:p.Lys179Glu | |
| ENST00000549111.5:n.646A>G | ||
| ENST00000551988.5:n.571A>G | ||
| ENST00000553106.5:c.550A>G | ENSP00000448059.1:p.Lys184Glu | |
| NM_000277.1:c.550A>G | NP_000268.1:p.Lys184Glu | |
| XM_011538422.1:c.550A>G | XP_011536724.1:p.Lys184Glu | |
| NM_000277.2:c.550A>G | NP_000268.1:p.Lys184Glu | |
| NM_001354304.1:c.550A>G | NP_001341233.1:p.Lys184Glu | |
| XM_017019370.2:c.550A>G | XP_016874859.1:p.Lys184Glu | |
| NM_000277.3:c.550A>G MANE Select | NP_000268.1:p.Lys184Glu | |
| NM_001354304.2:c.550A>G | NP_001341233.1:p.Lys184Glu |