HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65247625_65247626insG , CM000674.2:g.65247625_65247626insG | GRCh38 |
NC_000012.11:g.65641405_65641406insG , CM000674.1:g.65641405_65641406insG | GRCh37 |
NC_000012.10:g.63927672_63927673insG | NCBI36 |
NG_016210.1:g.83055_83056insG | |
NG_016210.2:g.83055_83056insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.*1300_*1301insG MANE Select | ENSP00000308369.2:n.*1300_*1301insG | |
ENST00000308330.2:c.*1300_*1301insG | ENSP00000308369.2:n.*1300_*1301insG | |
NM_001167614.1:c.*1300_*1301insG | NP_001161086.1:n.*1300_*1301insG | |
NM_014319.4:c.*1300_*1301insG | NP_055134.2:n.*1300_*1301insG | |
NM_014319.5:c.*1300_*1301insG MANE Select | NP_055134.2:n.*1300_*1301insG | |
NM_001167614.2:c.*1300_*1301insG | NP_001161086.1:n.*1300_*1301insG |