HGVS | Genome Assembly |
---|---|
NC_000011.10:g.55811662_55811663insGG , CM000673.2:g.55811662_55811663insGG | GRCh38 |
NC_000011.9:g.55579138_55579139insGG , CM000673.1:g.55579138_55579139insGG | GRCh37 |
NC_000011.8:g.55335714_55335715insGG | NCBI36 |
NG_052620.1:g.5296_5297insGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000625203.2:c.196_197insGG MANE Select | ENSP00000485319.1:p.Leu66TrpfsTer5 | |
ENST00000333973.3:c.196_197insGG | ENSP00000335529.2:p.Leu66TrpfsTer5 | |
ENST00000623450.1:c.196_197insGG | ENSP00000485509.1:p.Leu66TrpfsTer5 | |
ENST00000625203.1:c.196_197insGG | ENSP00000485319.1:p.Leu66TrpfsTer5 | |
NM_001004738.1:c.196_197insGG | NP_001004738.1:p.Leu66TrpfsTer5 | |
NM_001004738.2:c.196_197insGG MANE Select | NP_001004738.1:p.Leu66TrpfsTer5 |