HGVS | Genome Assembly |
---|---|
NC_000001.11:g.1014317_1014319delinsGGG , CM000663.2:g.1014317_1014319delinsGGG | GRCh38 |
NC_000001.10:g.949697_949699delinsGGG , CM000663.1:g.949697_949699delinsGGG | GRCh37 |
NC_000001.9:g.939560_939562delinsGGG | NCBI36 |
NG_033033.1:g.5851_5853delinsGGG | |
NG_033033.2:g.18180_18182delinsGGG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000624697.4:c.313_315delinsGGG | ENSP00000485643.1:p.Gly105= | |
ENST00000649529.1:c.337_339delinsGGG MANE Select | ENSP00000496832.1:p.Gly113= | |
ENST00000379389.4:c.337_339delinsGGG | ENSP00000368699.4:p.Gly113= | |
ENST00000624652.1:c.313_315delinsGGG | ENSP00000485313.1:p.Gly105= | |
ENST00000624697.3:c.313_315delinsGGG | ENSP00000485643.1:p.Gly105= | |
NM_005101.3:c.337_339delinsGGG | NP_005092.1:p.Gly113= | |
NM_005101.4:c.337_339delinsGGG MANE Select | NP_005092.1:p.Gly113= |