HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734034_4734035insG , CM000679.2:g.4734034_4734035insG | GRCh38 |
NC_000017.10:g.4637329_4637330insG , CM000679.1:g.4637329_4637330insG | GRCh37 |
NC_000017.9:g.4584078_4584079insG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*468_*469insC MANE Select | ENSP00000293778.7:n.*468_*469insC | |
ENST00000293778.10:c.*468_*469insC | ENSP00000293778.6:n.*468_*469insC | |
ENST00000576153.5:n.1024_1025insC | ||
NM_022059.3:c.*468_*469insC | NP_071342.2:n.*468_*469insC | |
NM_022059.4:c.*468_*469insC | NP_071342.2:n.*468_*469insC | |
NM_001386809.1:c.*468_*469insC MANE Select | NP_001373738.1:n.*468_*469insC |