HGVS | Genome Assembly |
---|---|
NC_000001.11:g.155290171_155290173delinsCTG , CM000663.2:g.155290171_155290173delinsCTG | GRCh38 |
NC_000001.10:g.155259962_155259964delinsCTG , CM000663.1:g.155259962_155259964delinsCTG | GRCh37 |
NC_000001.9:g.153526586_153526588delinsCTG | NCBI36 |
NG_011677.1:g.16262_16264delinsCAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000342741.6:c.*399_*401delinsCAG MANE Select | ENSP00000339933.4:n.*399_*401delinsCAG | |
ENST00000392414.7:c.*399_*401delinsCAG | ENSP00000376214.3:n.*399_*401delinsCAG | |
NM_000298.5:c.*399_*401delinsCAG | NP_000289.1:n.*399_*401delinsCAG | |
NM_181871.3:c.*399_*401delinsCAG | NP_870986.1:n.*399_*401delinsCAG | |
NM_000298.6:c.*399_*401delinsCAG MANE Select | NP_000289.1:n.*399_*401delinsCAG | |
NM_181871.4:c.*399_*401delinsCAG | NP_870986.1:n.*399_*401delinsCAG |