HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734192_4734194delinsCGA , CM000679.2:g.4734192_4734194delinsCGA | GRCh38 |
NC_000017.10:g.4637487_4637489delinsCGA , CM000679.1:g.4637487_4637489delinsCGA | GRCh37 |
NC_000017.9:g.4584236_4584238delinsCGA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*309_*311delinsTCG MANE Select | ENSP00000293778.7:n.*309_*311delinsTCG | |
ENST00000293778.10:c.*309_*311delinsTCG | ENSP00000293778.6:n.*309_*311delinsTCG | |
ENST00000576153.5:n.865_867delinsTCG | ||
NM_022059.3:c.*309_*311delinsTCG | NP_071342.2:n.*309_*311delinsTCG | |
NM_022059.4:c.*309_*311delinsTCG | NP_071342.2:n.*309_*311delinsTCG | |
NM_001386809.1:c.*309_*311delinsTCG MANE Select | NP_001373738.1:n.*309_*311delinsTCG |