Canonical Allele Identifier: CA1703612961
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145700G= , CM000669.2:g.44145700G= GRCh38
NC_000007.13:g.44185299G= , CM000669.1:g.44185299G= GRCh37
NC_000007.12:g.44151824G= NCBI36
NG_008847.1:g.48724C=
NG_008847.2:g.57471C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1048C= ENSP00000379142.4:n.*1048C=
ENST00000616242.5:c.*170C= ENSP00000482149.2:n.*170C=
ENST00000683378.1:n.276C=
ENST00000336642.9:c.84C= ENSP00000338009.5:p.Asn28=
ENST00000345378.7:c.1053C= ENSP00000223366.2:p.Asn351=
ENST00000403799.8:c.1050C= MANE Select ENSP00000384247.3:p.Asn350=
ENST00000671824.1:c.1113C= ENSP00000500264.1:p.Asn371=
ENST00000672743.1:n.62C=
ENST00000673284.1:c.1050C= ENSP00000499852.1:p.Asn350=
ENST00000336642.8:c.102C= ENSP00000338009.4:p.Asn34=
ENST00000345378.6:c.1053C= ENSP00000223366.2:p.Asn351=
ENST00000395796.7:c.1047C= ENSP00000379142.3:p.Asn349=
ENST00000403799.7:c.1050C= ENSP00000384247.3:p.Asn350=
ENST00000437084.1:c.999C= ENSP00000402840.1:p.Asn333=
ENST00000459642.1:n.430C=
ENST00000473353.1:n.348C=
ENST00000616242.4:c.1047C= ENSP00000482149.1:p.Asn349=
NM_000162.3:c.1050C= NP_000153.1:p.Asn350=
NM_033507.1:c.1053C= NP_277042.1:p.Asn351=
NM_033508.1:c.1047C= NP_277043.1:p.Asn349=
NM_000162.4:c.1050C= NP_000153.1:p.Asn350=
NM_001354800.1:c.1050C= NP_001341729.1:p.Asn350=
NM_001354801.1:c.39C= NP_001341730.1:p.Asn13=
NM_001354802.1:c.-91C= NP_001341731.1:n.-91C=
NM_001354803.1:c.84C= NP_001341732.1:p.Asn28=
NM_033507.2:c.1053C= NP_277042.1:p.Asn351=
NM_033508.2:c.1047C= NP_277043.1:p.Asn349=
XM_024446707.1:c.-91C= XP_024302475.1:n.-91C=
NM_000162.5:c.1050C= MANE Select NP_000153.1:p.Asn350=
NM_033507.3:c.1053C= NP_277042.1:p.Asn351=
NM_033508.3:c.1047C= NP_277043.1:p.Asn349=
NM_001354803.2:c.84C= NP_001341732.1:p.Asn28=