Canonical Allele Identifier: CA1703637541
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153367C= , CM000669.2:g.44153367C= GRCh38
NC_000007.13:g.44192966C= , CM000669.1:g.44192966C= GRCh37
NC_000007.12:g.44159491C= NCBI36
NG_008847.1:g.41057G=
NG_008847.2:g.49804G=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*140G= ENSP00000379142.4:n.*140G=
ENST00000616242.5:c.142G= ENSP00000482149.2:p.Glu48=
ENST00000682635.1:n.628G=
ENST00000345378.7:c.145G= ENSP00000223366.2:p.Glu49=
ENST00000403799.8:c.142G= MANE Select ENSP00000384247.3:p.Glu48=
ENST00000671824.1:c.142G= ENSP00000500264.1:p.Glu48=
ENST00000673284.1:c.142G= ENSP00000499852.1:p.Glu48=
ENST00000345378.6:c.145G= ENSP00000223366.2:p.Glu49=
ENST00000395796.7:c.139G= ENSP00000379142.3:p.Glu47=
ENST00000403799.7:c.142G= ENSP00000384247.3:p.Glu48=
ENST00000437084.1:c.142G= ENSP00000402840.1:p.Glu48=
ENST00000616242.4:c.139G= ENSP00000482149.1:p.Glu47=
NM_000162.3:c.142G= NP_000153.1:p.Glu48=
NM_033507.1:c.145G= NP_277042.1:p.Glu49=
NM_033508.1:c.139G= NP_277043.1:p.Glu47=
NM_000162.4:c.142G= NP_000153.1:p.Glu48=
NM_001354800.1:c.142G= NP_001341729.1:p.Glu48=
NM_033507.2:c.145G= NP_277042.1:p.Glu49=
NM_033508.2:c.139G= NP_277043.1:p.Glu47=
NM_000162.5:c.142G= MANE Select NP_000153.1:p.Glu48=
NM_033507.3:c.145G= NP_277042.1:p.Glu49=
NM_033508.3:c.139G= NP_277043.1:p.Glu47=