Canonical Allele Identifier: CA1703613475

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146509G= , CM000669.2:g.44146509G=	GRCh38
NC_000007.13:g.44186108G= , CM000669.1:g.44186108G=	GRCh37
NC_000007.12:g.44152633G=	NCBI36
NG_008847.1:g.47915C=
NG_008847.2:g.56662C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*971C=	ENSP00000379142.4:n.*971C=
ENST00000616242.5:c.*93C=	ENSP00000482149.2:n.*93C=
ENST00000683378.1:n.199C=
ENST00000345378.7:c.976C=	ENSP00000223366.2:p.Arg326=
ENST00000403799.8:c.973C= MANE Select	ENSP00000384247.3:p.Arg325=
ENST00000671824.1:c.1036C=	ENSP00000500264.1:p.Arg346=
ENST00000673284.1:c.973C=	ENSP00000499852.1:p.Arg325=
ENST00000345378.6:c.976C=	ENSP00000223366.2:p.Arg326=
ENST00000395796.7:c.970C=	ENSP00000379142.3:p.Arg324=
ENST00000403799.7:c.973C=	ENSP00000384247.3:p.Arg325=
ENST00000437084.1:c.922C=	ENSP00000402840.1:p.Arg308=
ENST00000473353.1:n.271C=
ENST00000616242.4:c.970C=	ENSP00000482149.1:p.Arg324=
NM_000162.3:c.973C=	NP_000153.1:p.Arg325=
NM_033507.1:c.976C=	NP_277042.1:p.Arg326=
NM_033508.1:c.970C=	NP_277043.1:p.Arg324=
NM_000162.4:c.973C=	NP_000153.1:p.Arg325=
NM_001354800.1:c.973C=	NP_001341729.1:p.Arg325=
NM_001354801.1:c.8+110C=	NP_001341730.1:n.8+110C=
NM_033507.2:c.976C=	NP_277042.1:p.Arg326=
NM_033508.2:c.970C=	NP_277043.1:p.Arg324=
NM_000162.5:c.973C= MANE Select	NP_000153.1:p.Arg325=
NM_033507.3:c.976C=	NP_277042.1:p.Arg326=
NM_033508.3:c.970C=	NP_277043.1:p.Arg324=