HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148994600_148994604delinsATGGT , CM000667.2:g.148994600_148994604delinsATGGT | GRCh38 |
NC_000005.9:g.148374163_148374167delinsATGGT , CM000667.1:g.148374163_148374167delinsATGGT | GRCh37 |
NC_000005.8:g.148354356_148354360delinsATGGT | NCBI36 |
NG_007947.2:g.73571_73575delinsACCAT , LRG_269:g.73571_73575delinsACCAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000515425.6:c.*10107_*10111delinsACCAT MANE Select | ENSP00000423660.1:n.*10107_*10111delinsACCAT | |
ENST00000504690.5:c.*12+9122_*12+9126delinsACCAT | ENSP00000425627.1:n.*12+9122_*12+9126delinsACCAT | |
ENST00000510350.1:n.231+12277_231+12281delinsACCAT | ||
NM_024577.3:c.*10107_*10111delinsACCAT , LRG_269t1:c.*10107_*10111delinsACCAT | NP_078853.2:n.*10107_*10111delinsACCAT | |
NM_024577.4:c.*10107_*10111delinsACCAT MANE Select | NP_078853.2:n.*10107_*10111delinsACCAT |