Canonical Allele Identifier: CA1703612969
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145720C= , CM000669.2:g.44145720C= GRCh38
NC_000007.13:g.44185319C= , CM000669.1:g.44185319C= GRCh37
NC_000007.12:g.44151844C= NCBI36
NG_008847.1:g.48704G=
NG_008847.2:g.57451G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1028G= ENSP00000379142.4:n.*1028G=
ENST00000616242.5:c.*150G= ENSP00000482149.2:n.*150G=
ENST00000683378.1:n.256G=
ENST00000336642.9:c.64G= ENSP00000338009.5:p.Asp22=
ENST00000345378.7:c.1033G= ENSP00000223366.2:p.Asp345=
ENST00000403799.8:c.1030G= MANE Select ENSP00000384247.3:p.Asp344=
ENST00000671824.1:c.1093G= ENSP00000500264.1:p.Asp365=
ENST00000672743.1:n.42G=
ENST00000673284.1:c.1030G= ENSP00000499852.1:p.Asp344=
ENST00000336642.8:c.82G= ENSP00000338009.4:p.Asp28=
ENST00000345378.6:c.1033G= ENSP00000223366.2:p.Asp345=
ENST00000395796.7:c.1027G= ENSP00000379142.3:p.Asp343=
ENST00000403799.7:c.1030G= ENSP00000384247.3:p.Asp344=
ENST00000437084.1:c.979G= ENSP00000402840.1:p.Asp327=
ENST00000459642.1:n.410G=
ENST00000473353.1:n.328G=
ENST00000616242.4:c.1027G= ENSP00000482149.1:p.Asp343=
NM_000162.3:c.1030G= NP_000153.1:p.Asp344=
NM_033507.1:c.1033G= NP_277042.1:p.Asp345=
NM_033508.1:c.1027G= NP_277043.1:p.Asp343=
NM_000162.4:c.1030G= NP_000153.1:p.Asp344=
NM_001354800.1:c.1030G= NP_001341729.1:p.Asp344=
NM_001354801.1:c.19G= NP_001341730.1:p.Asp7=
NM_001354802.1:c.-111G= NP_001341731.1:n.-111G=
NM_001354803.1:c.64G= NP_001341732.1:p.Asp22=
NM_033507.2:c.1033G= NP_277042.1:p.Asp345=
NM_033508.2:c.1027G= NP_277043.1:p.Asp343=
XM_024446707.1:c.-111G= XP_024302475.1:n.-111G=
NM_000162.5:c.1030G= MANE Select NP_000153.1:p.Asp344=
NM_033507.3:c.1033G= NP_277042.1:p.Asp345=
NM_033508.3:c.1027G= NP_277043.1:p.Asp343=
NM_001354803.2:c.64G= NP_001341732.1:p.Asp22=