HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734070_4734071insCTG , CM000679.2:g.4734070_4734071insCTG | GRCh38 |
NC_000017.10:g.4637365_4637366insCTG , CM000679.1:g.4637365_4637366insCTG | GRCh37 |
NC_000017.9:g.4584114_4584115insCTG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*434_*435insGCA MANE Select | ENSP00000293778.7:n.*434_*435insGCA | |
ENST00000293778.10:c.*434_*435insGCA | ENSP00000293778.6:n.*434_*435insGCA | |
ENST00000576153.5:n.990_991insGCA | ||
NM_022059.3:c.*434_*435insGCA | NP_071342.2:n.*434_*435insGCA | |
NM_022059.4:c.*434_*435insGCA | NP_071342.2:n.*434_*435insGCA | |
NM_001386809.1:c.*434_*435insGCA MANE Select | NP_001373738.1:n.*434_*435insGCA |