Canonical Allele Identifier: CA1703612679

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145216C= , CM000669.2:g.44145216C=	GRCh38
NC_000007.13:g.44184815C= , CM000669.1:g.44184815C=	GRCh37
NC_000007.12:g.44151340C=	NCBI36
NG_008847.1:g.49208G=
NG_008847.2:g.57955G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1316G=	ENSP00000379142.4:n.*1316G=
ENST00000616242.5:c.*438G=	ENSP00000482149.2:n.*438G=
ENST00000683378.1:n.544G=
ENST00000336642.9:c.352G=	ENSP00000338009.5:p.Glu118=
ENST00000345378.7:c.1321G=	ENSP00000223366.2:p.Glu441=
ENST00000403799.8:c.1318G= MANE Select	ENSP00000384247.3:p.Glu440=
ENST00000671824.1:c.1381G=	ENSP00000500264.1:p.Glu461=
ENST00000672743.1:n.330G=
ENST00000673284.1:c.1318G=	ENSP00000499852.1:p.Glu440=
ENST00000336642.8:c.370G=	ENSP00000338009.4:p.Glu124=
ENST00000345378.6:c.1321G=	ENSP00000223366.2:p.Glu441=
ENST00000395796.7:c.1315G=	ENSP00000379142.3:p.Glu439=
ENST00000403799.7:c.1318G=	ENSP00000384247.3:p.Glu440=
ENST00000437084.1:c.1267G=	ENSP00000402840.1:p.Glu423=
ENST00000459642.1:n.698G=
ENST00000616242.4:c.1315G=	ENSP00000482149.1:p.Glu439=
NM_000162.3:c.1318G=	NP_000153.1:p.Glu440=
NM_033507.1:c.1321G=	NP_277042.1:p.Glu441=
NM_033508.1:c.1315G=	NP_277043.1:p.Glu439=
NM_000162.4:c.1318G=	NP_000153.1:p.Glu440=
NM_001354800.1:c.1318G=	NP_001341729.1:p.Glu440=
NM_001354801.1:c.307G=	NP_001341730.1:p.Glu103=
NM_001354802.1:c.178G=	NP_001341731.1:p.Glu60=
NM_001354803.1:c.352G=	NP_001341732.1:p.Glu118=
NM_033507.2:c.1321G=	NP_277042.1:p.Glu441=
NM_033508.2:c.1315G=	NP_277043.1:p.Glu439=
XM_024446707.1:c.178G=	XP_024302475.1:p.Glu60=
NM_000162.5:c.1318G= MANE Select	NP_000153.1:p.Glu440=
NM_033507.3:c.1321G=	NP_277042.1:p.Glu441=
NM_033508.3:c.1315G=	NP_277043.1:p.Glu439=
NM_001354803.2:c.352G=	NP_001341732.1:p.Glu118=