HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186086062_186086063insT , CM000666.2:g.186086062_186086063insT | GRCh38 |
NC_000004.11:g.187007216_187007217insT , CM000666.1:g.187007216_187007217insT | GRCh37 |
NC_000004.10:g.187244210_187244211insT | NCBI36 |
NG_007278.1:g.21908_21909insT , LRG_117:g.21908_21909insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3456_*3457insT | ENSP00000513675.1:n.*3456_*3457insT | |
ENST00000698353.1:n.3779_3780insT | ||
ENST00000698354.1:c.*1189_*1190insT | ENSP00000513676.1:n.*1189_*1190insT | |
ENST00000296795.8:c.*1189_*1190insT MANE Select | ENSP00000296795.3:n.*1189_*1190insT | |
ENST00000296795.7:c.*1189_*1190insT | ENSP00000296795.2:n.*1189_*1190insT | |
NM_003265.3:c.*1189_*1190insT MANE Select | NP_003256.1:n.*1189_*1190insT |