Canonical Allele Identifier: CA1703612855
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145521C= , CM000669.2:g.44145521C= GRCh38
NC_000007.13:g.44185120C= , CM000669.1:g.44185120C= GRCh37
NC_000007.12:g.44151645C= NCBI36
NG_008847.1:g.48903G=
NG_008847.2:g.57650G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1227G= ENSP00000379142.4:n.*1227G=
ENST00000616242.5:c.*349G= ENSP00000482149.2:n.*349G=
ENST00000683378.1:n.455G=
ENST00000336642.9:c.263G= ENSP00000338009.5:p.Gly88=
ENST00000345378.7:c.1232G= ENSP00000223366.2:p.Gly411=
ENST00000403799.8:c.1229G= MANE Select ENSP00000384247.3:p.Gly410=
ENST00000671824.1:c.1292G= ENSP00000500264.1:p.Gly431=
ENST00000672743.1:n.241G=
ENST00000673284.1:c.1229G= ENSP00000499852.1:p.Gly410=
ENST00000336642.8:c.281G= ENSP00000338009.4:p.Gly94=
ENST00000345378.6:c.1232G= ENSP00000223366.2:p.Gly411=
ENST00000395796.7:c.1226G= ENSP00000379142.3:p.Gly409=
ENST00000403799.7:c.1229G= ENSP00000384247.3:p.Gly410=
ENST00000437084.1:c.1178G= ENSP00000402840.1:p.Gly393=
ENST00000459642.1:n.609G=
ENST00000616242.4:c.1226G= ENSP00000482149.1:p.Gly409=
NM_000162.3:c.1229G= NP_000153.1:p.Gly410=
NM_033507.1:c.1232G= NP_277042.1:p.Gly411=
NM_033508.1:c.1226G= NP_277043.1:p.Gly409=
NM_000162.4:c.1229G= NP_000153.1:p.Gly410=
NM_001354800.1:c.1229G= NP_001341729.1:p.Gly410=
NM_001354801.1:c.218G= NP_001341730.1:p.Gly73=
NM_001354802.1:c.89G= NP_001341731.1:p.Gly30=
NM_001354803.1:c.263G= NP_001341732.1:p.Gly88=
NM_033507.2:c.1232G= NP_277042.1:p.Gly411=
NM_033508.2:c.1226G= NP_277043.1:p.Gly409=
XM_024446707.1:c.89G= XP_024302475.1:p.Gly30=
NM_000162.5:c.1229G= MANE Select NP_000153.1:p.Gly410=
NM_033507.3:c.1232G= NP_277042.1:p.Gly411=
NM_033508.3:c.1226G= NP_277043.1:p.Gly409=
NM_001354803.2:c.263G= NP_001341732.1:p.Gly88=