HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734036_4734037insT , CM000679.2:g.4734036_4734037insT | GRCh38 |
NC_000017.10:g.4637331_4637332insT , CM000679.1:g.4637331_4637332insT | GRCh37 |
NC_000017.9:g.4584080_4584081insT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*466_*467insA MANE Select | ENSP00000293778.7:n.*466_*467insA | |
ENST00000293778.10:c.*466_*467insA | ENSP00000293778.6:n.*466_*467insA | |
ENST00000576153.5:n.1022_1023insA | ||
NM_022059.3:c.*466_*467insA | NP_071342.2:n.*466_*467insA | |
NM_022059.4:c.*466_*467insA | NP_071342.2:n.*466_*467insA | |
NM_001386809.1:c.*466_*467insA MANE Select | NP_001373738.1:n.*466_*467insA |