Canonical Allele Identifier: CA1703613477

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146514T= , CM000669.2:g.44146514T=	GRCh38
NC_000007.13:g.44186113T= , CM000669.1:g.44186113T=	GRCh37
NC_000007.12:g.44152638T=	NCBI36
NG_008847.1:g.47910A=
NG_008847.2:g.56657A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*966A=	ENSP00000379142.4:n.*966A=
ENST00000616242.5:c.*88A=	ENSP00000482149.2:n.*88A=
ENST00000683378.1:n.194A=
ENST00000345378.7:c.971A=	ENSP00000223366.2:p.Gln324=
ENST00000403799.8:c.968A= MANE Select	ENSP00000384247.3:p.Gln323=
ENST00000671824.1:c.1031A=	ENSP00000500264.1:p.Gln344=
ENST00000673284.1:c.968A=	ENSP00000499852.1:p.Gln323=
ENST00000345378.6:c.971A=	ENSP00000223366.2:p.Gln324=
ENST00000395796.7:c.965A=	ENSP00000379142.3:p.Gln322=
ENST00000403799.7:c.968A=	ENSP00000384247.3:p.Gln323=
ENST00000437084.1:c.917A=	ENSP00000402840.1:p.Gln306=
ENST00000473353.1:n.266A=
ENST00000616242.4:c.965A=	ENSP00000482149.1:p.Gln322=
NM_000162.3:c.968A=	NP_000153.1:p.Gln323=
NM_033507.1:c.971A=	NP_277042.1:p.Gln324=
NM_033508.1:c.965A=	NP_277043.1:p.Gln322=
NM_000162.4:c.968A=	NP_000153.1:p.Gln323=
NM_001354800.1:c.968A=	NP_001341729.1:p.Gln323=
NM_001354801.1:c.8+105A=	NP_001341730.1:n.8+105A=
NM_033507.2:c.971A=	NP_277042.1:p.Gln324=
NM_033508.2:c.965A=	NP_277043.1:p.Gln322=
NM_000162.5:c.968A= MANE Select	NP_000153.1:p.Gln323=
NM_033507.3:c.971A=	NP_277042.1:p.Gln324=
NM_033508.3:c.965A=	NP_277043.1:p.Gln322=