HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4631290_4631291insGG , CM000679.2:g.4631290_4631291insGG | GRCh38 |
NC_000017.10:g.4534585_4534586insGG , CM000679.1:g.4534585_4534586insGG | GRCh37 |
NC_000017.9:g.4481334_4481335insGG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293761.8:c.*309_*310insCC MANE Select | ENSP00000293761.3:n.*309_*310insCC | |
ENST00000293761.7:c.*309_*310insCC | ENSP00000293761.3:n.*309_*310insCC | |
ENST00000570836.5:c.*309_*310insCC | ENSP00000458832.1:n.*309_*310insCC | |
NM_001140.3:c.*309_*310insCC | NP_001131.3:n.*309_*310insCC | |
NM_001140.4:c.*309_*310insCC | NP_001131.3:n.*309_*310insCC | |
NM_001140.5:c.*309_*310insCC MANE Select | NP_001131.3:n.*309_*310insCC |