HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085294_186085296delinsAAT , CM000666.2:g.186085294_186085296delinsAAT | GRCh38 |
NC_000004.11:g.187006448_187006450delinsAAT , CM000666.1:g.187006448_187006450delinsAAT | GRCh37 |
NC_000004.10:g.187243442_187243444delinsAAT | NCBI36 |
NG_007278.1:g.21140_21142delinsAAT , LRG_117:g.21140_21142delinsAAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*2688_*2690delinsAAT | ENSP00000513675.1:n.*2688_*2690delinsAAT | |
ENST00000698353.1:n.3011_3013delinsAAT | ||
ENST00000698354.1:c.*421_*423delinsAAT | ENSP00000513676.1:n.*421_*423delinsAAT | |
ENST00000296795.8:c.*421_*423delinsAAT MANE Select | ENSP00000296795.3:n.*421_*423delinsAAT | |
ENST00000296795.7:c.*421_*423delinsAAT | ENSP00000296795.2:n.*421_*423delinsAAT | |
NM_003265.3:c.*421_*423delinsAAT MANE Select | NP_003256.1:n.*421_*423delinsAAT |