Canonical Allele Identifier: CA1703637532

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153355C= , CM000669.2:g.44153355C=	GRCh38
NC_000007.13:g.44192954C= , CM000669.1:g.44192954C=	GRCh37
NC_000007.12:g.44159479C=	NCBI36
NG_008847.1:g.41069G=
NG_008847.2:g.49816G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*152G=	ENSP00000379142.4:n.*152G=
ENST00000616242.5:c.154G=	ENSP00000482149.2:p.Glu52=
ENST00000682635.1:n.640G=
ENST00000345378.7:c.157G=	ENSP00000223366.2:p.Glu53=
ENST00000403799.8:c.154G= MANE Select	ENSP00000384247.3:p.Glu52=
ENST00000671824.1:c.154G=	ENSP00000500264.1:p.Glu52=
ENST00000673284.1:c.154G=	ENSP00000499852.1:p.Glu52=
ENST00000345378.6:c.157G=	ENSP00000223366.2:p.Glu53=
ENST00000395796.7:c.151G=	ENSP00000379142.3:p.Glu51=
ENST00000403799.7:c.154G=	ENSP00000384247.3:p.Glu52=
ENST00000437084.1:c.154G=	ENSP00000402840.1:p.Glu52=
ENST00000616242.4:c.151G=	ENSP00000482149.1:p.Glu51=
NM_000162.3:c.154G=	NP_000153.1:p.Glu52=
NM_033507.1:c.157G=	NP_277042.1:p.Glu53=
NM_033508.1:c.151G=	NP_277043.1:p.Glu51=
NM_000162.4:c.154G=	NP_000153.1:p.Glu52=
NM_001354800.1:c.154G=	NP_001341729.1:p.Glu52=
NM_033507.2:c.157G=	NP_277042.1:p.Glu53=
NM_033508.2:c.151G=	NP_277043.1:p.Glu51=
NM_000162.5:c.154G= MANE Select	NP_000153.1:p.Glu52=
NM_033507.3:c.157G=	NP_277042.1:p.Glu53=
NM_033508.3:c.151G=	NP_277043.1:p.Glu51=