HGVS | Genome Assembly |
---|---|
NC_000005.10:g.52864962_52864963insG , CM000667.2:g.52864962_52864963insG | GRCh38 |
NC_000005.9:g.52160796_52160797insG , CM000667.1:g.52160796_52160797insG | GRCh37 |
NC_000005.8:g.52196553_52196554insG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000282588.7:c.385-9_385-8insG MANE Select | ENSP00000282588.5:n.385-9_385-8insG | |
ENST00000650673.1:c.385-9_385-8insG | ENSP00000498529.1:n.385-9_385-8insG | |
ENST00000282588.6:c.385-9_385-8insG | ENSP00000282588.5:n.385-9_385-8insG | |
ENST00000513737.5:n.136-9_136-8insG | ||
ENST00000514262.5:n.136-9_136-8insG | ||
NM_181501.1:c.385-9_385-8insG | NP_852478.1:n.385-9_385-8insG | |
NM_181501.2:c.385-9_385-8insG MANE Select | NP_852478.1:n.385-9_385-8insG |