HGVS | Genome Assembly |
---|---|
NC_000012.12:g.52519853_52519855delinsACT , CM000674.2:g.52519853_52519855delinsACT | GRCh38 |
NC_000012.11:g.52913637_52913639delinsACT , CM000674.1:g.52913637_52913639delinsACT | GRCh37 |
NC_000012.10:g.51199904_51199906delinsACT | NCBI36 |
NG_008297.1:g.5605_5607delinsAGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000252242.9:c.442_444delinsAGT MANE Select | ENSP00000252242.4:p.Ser148= | |
ENST00000252242.8:c.442_444delinsAGT | ENSP00000252242.4:p.Ser148= | |
ENST00000549420.1:c.112_114delinsAGT | ENSP00000447209.1:p.Ser38= | |
ENST00000551275.1:c.337_339delinsAGT | ENSP00000448041.1:p.Ser113= | |
ENST00000552629.5:n.540_542delinsAGT | ||
NM_000424.3:c.442_444delinsAGT | NP_000415.2:p.Ser148= | |
NM_000424.4:c.442_444delinsAGT MANE Select | NP_000415.2:p.Ser148= |