HGVS | Genome Assembly |
---|---|
NC_000002.12:g.43886648_43886649insCTG , CM000664.2:g.43886648_43886649insCTG | GRCh38 |
NC_000002.11:g.44113787_44113788insCTG , CM000664.1:g.44113787_44113788insCTG | GRCh37 |
NC_000002.10:g.43967291_43967292insCTG | NCBI36 |
NG_008247.1:g.114359_114360insGCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000682612.1:c.2905_2906insGCA | ||
ENST00000684454.1:n.10002_10003insGCA | ||
ENST00000260665.12:c.*1953_*1954insGCA MANE Select | ENSP00000260665.7:n.*1953_*1954insGCA | |
ENST00000260665.11:c.*1953_*1954insGCA | ENSP00000260665.7:n.*1953_*1954insGCA | |
NM_133259.3:c.*1953_*1954insGCA | NP_573566.2:n.*1953_*1954insGCA | |
XR_002958896.1:n.6320_6321insGCA | ||
NM_133259.4:c.*1953_*1954insGCA MANE Select | NP_573566.2:n.*1953_*1954insGCA |