HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4631289_4631290insCC , CM000679.2:g.4631289_4631290insCC | GRCh38 |
NC_000017.10:g.4534584_4534585insCC , CM000679.1:g.4534584_4534585insCC | GRCh37 |
NC_000017.9:g.4481333_4481334insCC | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293761.8:c.*310_*311insGG MANE Select | ENSP00000293761.3:n.*310_*311insGG | |
ENST00000293761.7:c.*310_*311insGG | ENSP00000293761.3:n.*310_*311insGG | |
ENST00000570836.5:c.*310_*311insGG | ENSP00000458832.1:n.*310_*311insGG | |
NM_001140.3:c.*310_*311insGG | NP_001131.3:n.*310_*311insGG | |
NM_001140.4:c.*310_*311insGG | NP_001131.3:n.*310_*311insGG | |
NM_001140.5:c.*310_*311insGG MANE Select | NP_001131.3:n.*310_*311insGG |