Revel Score:
ENST00000284885 (MANE Select)
0.106
gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.18359856G>C , CM000683.2:g.18359856G>C | GRCh38 |
| NC_000021.8:g.19732173G>C , CM000683.1:g.19732173G>C | GRCh37 |
| NC_000021.7:g.18654044G>C | NCBI36 |
| NG_012207.1:g.48798C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284885.8:c.781C>G MANE Select | ENSP00000284885.3:p.Gln261Glu | |
| ENST00000284885.7:c.781C>G | ENSP00000284885.3:p.Gln261Glu | |
| NM_002772.2:c.781C>G | NP_002763.2:p.Gln261Glu | |
| XM_011529654.1:c.916C>G | XP_011527956.1:p.Gln306Glu | |
| XM_011529655.1:c.916C>G | XP_011527957.1:p.Gln306Glu | |
| XM_011529656.1:c.916C>G | XP_011527958.1:p.Gln306Glu | |
| XM_011529657.1:c.871C>G | XP_011527959.1:p.Gln291Glu | |
| XM_011529658.1:c.835C>G | XP_011527960.1:p.Gln279Glu | |
| XM_011529659.1:c.826C>G | XP_011527961.1:p.Gln276Glu | |
| XM_011529654.2:c.916C>G | XP_011527956.1:p.Gln306Glu | |
| XM_011529656.2:c.916C>G | XP_011527958.1:p.Gln306Glu | |
| XM_011529657.2:c.871C>G | XP_011527959.1:p.Gln291Glu | |
| XM_011529658.2:c.835C>G | XP_011527960.1:p.Gln279Glu | |
| NM_002772.3:c.781C>G MANE Select | NP_002763.3:p.Gln261Glu |