Canonical Allele Identifier: CA1703613478

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146518C= , CM000669.2:g.44146518C=	GRCh38
NC_000007.13:g.44186117C= , CM000669.1:g.44186117C=	GRCh37
NC_000007.12:g.44152642C=	NCBI36
NG_008847.1:g.47906G=
NG_008847.2:g.56653G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*962G=	ENSP00000379142.4:n.*962G=
ENST00000616242.5:c.*84G=	ENSP00000482149.2:n.*84G=
ENST00000683378.1:n.190G=
ENST00000345378.7:c.967G=	ENSP00000223366.2:p.Glu323=
ENST00000403799.8:c.964G= MANE Select	ENSP00000384247.3:p.Glu322=
ENST00000671824.1:c.1027G=	ENSP00000500264.1:p.Glu343=
ENST00000673284.1:c.964G=	ENSP00000499852.1:p.Glu322=
ENST00000345378.6:c.967G=	ENSP00000223366.2:p.Glu323=
ENST00000395796.7:c.961G=	ENSP00000379142.3:p.Glu321=
ENST00000403799.7:c.964G=	ENSP00000384247.3:p.Glu322=
ENST00000437084.1:c.913G=	ENSP00000402840.1:p.Glu305=
ENST00000473353.1:n.262G=
ENST00000616242.4:c.961G=	ENSP00000482149.1:p.Glu321=
NM_000162.3:c.964G=	NP_000153.1:p.Glu322=
NM_033507.1:c.967G=	NP_277042.1:p.Glu323=
NM_033508.1:c.961G=	NP_277043.1:p.Glu321=
NM_000162.4:c.964G=	NP_000153.1:p.Glu322=
NM_001354800.1:c.964G=	NP_001341729.1:p.Glu322=
NM_001354801.1:c.8+101G=	NP_001341730.1:n.8+101G=
NM_033507.2:c.967G=	NP_277042.1:p.Glu323=
NM_033508.2:c.961G=	NP_277043.1:p.Glu321=
NM_000162.5:c.964G= MANE Select	NP_000153.1:p.Glu322=
NM_033507.3:c.967G=	NP_277042.1:p.Glu323=
NM_033508.3:c.961G=	NP_277043.1:p.Glu321=