Canonical Allele Identifier: CA1703612932
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145634C= , CM000669.2:g.44145634C= GRCh38
NC_000007.13:g.44185233C= , CM000669.1:g.44185233C= GRCh37
NC_000007.12:g.44151758C= NCBI36
NG_008847.1:g.48790G=
NG_008847.2:g.57537G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1114G= ENSP00000379142.4:n.*1114G=
ENST00000616242.5:c.*236G= ENSP00000482149.2:n.*236G=
ENST00000683378.1:n.342G=
ENST00000336642.9:c.150G= ENSP00000338009.5:p.Glu50=
ENST00000345378.7:c.1119G= ENSP00000223366.2:p.Glu373=
ENST00000403799.8:c.1116G= MANE Select ENSP00000384247.3:p.Glu372=
ENST00000671824.1:c.1179G= ENSP00000500264.1:p.Glu393=
ENST00000672743.1:n.128G=
ENST00000673284.1:c.1116G= ENSP00000499852.1:p.Glu372=
ENST00000336642.8:c.168G= ENSP00000338009.4:p.Glu56=
ENST00000345378.6:c.1119G= ENSP00000223366.2:p.Glu373=
ENST00000395796.7:c.1113G= ENSP00000379142.3:p.Glu371=
ENST00000403799.7:c.1116G= ENSP00000384247.3:p.Glu372=
ENST00000437084.1:c.1065G= ENSP00000402840.1:p.Glu355=
ENST00000459642.1:n.496G=
ENST00000616242.4:c.1113G= ENSP00000482149.1:p.Glu371=
NM_000162.3:c.1116G= NP_000153.1:p.Glu372=
NM_033507.1:c.1119G= NP_277042.1:p.Glu373=
NM_033508.1:c.1113G= NP_277043.1:p.Glu371=
NM_000162.4:c.1116G= NP_000153.1:p.Glu372=
NM_001354800.1:c.1116G= NP_001341729.1:p.Glu372=
NM_001354801.1:c.105G= NP_001341730.1:p.Glu35=
NM_001354802.1:c.-25G= NP_001341731.1:n.-25G=
NM_001354803.1:c.150G= NP_001341732.1:p.Glu50=
NM_033507.2:c.1119G= NP_277042.1:p.Glu373=
NM_033508.2:c.1113G= NP_277043.1:p.Glu371=
XM_024446707.1:c.-25G= XP_024302475.1:n.-25G=
NM_000162.5:c.1116G= MANE Select NP_000153.1:p.Glu372=
NM_033507.3:c.1119G= NP_277042.1:p.Glu373=
NM_033508.3:c.1113G= NP_277043.1:p.Glu371=
NM_001354803.2:c.150G= NP_001341732.1:p.Glu50=