HGVS | Genome Assembly |
---|---|
NC_000012.12:g.65247700_65247701delinsCT , CM000674.2:g.65247700_65247701delinsCT | GRCh38 |
NC_000012.11:g.65641480_65641481delinsCT , CM000674.1:g.65641480_65641481delinsCT | GRCh37 |
NC_000012.10:g.63927747_63927748delinsCT | NCBI36 |
NG_016210.1:g.83130_83131delinsCT | |
NG_016210.2:g.83130_83131delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308330.3:c.*1375_*1376delinsCT MANE Select | ENSP00000308369.2:n.*1375_*1376delinsCT | |
ENST00000308330.2:c.*1375_*1376delinsCT | ENSP00000308369.2:n.*1375_*1376delinsCT | |
NM_001167614.1:c.*1375_*1376delinsCT | NP_001161086.1:n.*1375_*1376delinsCT | |
NM_014319.4:c.*1375_*1376delinsCT | NP_055134.2:n.*1375_*1376delinsCT | |
NM_014319.5:c.*1375_*1376delinsCT MANE Select | NP_055134.2:n.*1375_*1376delinsCT | |
NM_001167614.2:c.*1375_*1376delinsCT | NP_001161086.1:n.*1375_*1376delinsCT |