Revel Score:
ENST00000299644
0.066
ENST00000408984
0.475
gnomAD v2:
gnomAD v3:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.78425054C>G , CM000678.2:g.78425054C>G | GRCh38 |
| NC_000016.9:g.78458951C>G , CM000678.1:g.78458951C>G | GRCh37 |
| NC_000016.8:g.77016452C>G | NCBI36 |
| NG_011698.1:g.330401C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000627394.3:c.790C>G | ENSP00000485925.2:p.Arg264Gly | |
| ENST00000683929.1:c.790C>G | ENSP00000507689.1:p.Arg264Gly | |
| ENST00000684632.1:n.1169C>G | ||
| ENST00000566780.6:c.790C>G MANE Select | ENSP00000457230.1:p.Arg264Gly | |
| ENST00000402655.6:c.409+309900C>G | ENSP00000384238.2:n.409+309900C>G | |
| ENST00000406884.6:c.516+260765C>G | ENSP00000384495.2:n.516+260765C>G | |
| ENST00000408984.7:c.790C>G | ENSP00000386161.3:p.Arg264Gly | |
| ENST00000539474.6:c.409+309900C>G | ENSP00000445210.2:n.409+309900C>G | |
| ENST00000562639.5:n.478C>G | ||
| ENST00000566780.5:c.790C>G | ENSP00000457230.1:p.Arg264Gly | |
| ENST00000569332.5:c.*587C>G | ENSP00000454788.1:n.*587C>G | |
| ENST00000620008.1:c.184C>G | ENSP00000482648.1:p.Arg62Gly | |
| NM_001291997.1:c.451C>G | NP_001278926.1:p.Arg151Gly | |
| NM_016373.3:c.790C>G | NP_057457.1:p.Arg264Gly | |
| XM_006721195.2:c.790C>G | XP_006721258.1:p.Arg264Gly | |
| XM_011523100.1:c.790C>G | XP_011521402.1:p.Arg264Gly | |
| XM_011523101.1:c.790C>G | XP_011521403.1:p.Arg264Gly | |
| XM_011523102.1:c.790C>G | XP_011521404.1:p.Arg264Gly | |
| XM_011523103.1:c.790C>G | XP_011521405.1:p.Arg264Gly | |
| XM_011523104.1:c.790C>G | XP_011521406.1:p.Arg264Gly | |
| XR_933765.1:n.3806+5372G>C | ||
| XM_011523101.3:c.790C>G | XP_011521403.1:p.Arg264Gly | |
| XM_011523103.3:c.790C>G | XP_011521405.1:p.Arg264Gly | |
| XM_011523104.3:c.790C>G | XP_011521406.1:p.Arg264Gly | |
| NM_016373.4:c.790C>G MANE Select | NP_057457.1:p.Arg264Gly | |
| NM_001291997.2:c.451C>G | NP_001278926.1:p.Arg151Gly |