Canonical Allele Identifier: CA1703613499

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146564C= , CM000669.2:g.44146564C=	GRCh38
NC_000007.13:g.44186163C= , CM000669.1:g.44186163C=	GRCh37
NC_000007.12:g.44152688C=	NCBI36
NG_008847.1:g.47860G=
NG_008847.2:g.56607G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*916G=	ENSP00000379142.4:n.*916G=
ENST00000616242.5:c.*38G=	ENSP00000482149.2:n.*38G=
ENST00000683378.1:n.144G=
ENST00000345378.7:c.921G=	ENSP00000223366.2:p.Leu307=
ENST00000403799.8:c.918G= MANE Select	ENSP00000384247.3:p.Leu306=
ENST00000671824.1:c.981G=	ENSP00000500264.1:p.Leu327=
ENST00000673284.1:c.918G=	ENSP00000499852.1:p.Leu306=
ENST00000345378.6:c.921G=	ENSP00000223366.2:p.Leu307=
ENST00000395796.7:c.915G=	ENSP00000379142.3:p.Leu305=
ENST00000403799.7:c.918G=	ENSP00000384247.3:p.Leu306=
ENST00000437084.1:c.867G=	ENSP00000402840.1:p.Leu289=
ENST00000473353.1:n.216G=
ENST00000616242.4:c.915G=	ENSP00000482149.1:p.Leu305=
NM_000162.3:c.918G=	NP_000153.1:p.Leu306=
NM_033507.1:c.921G=	NP_277042.1:p.Leu307=
NM_033508.1:c.915G=	NP_277043.1:p.Leu305=
NM_000162.4:c.918G=	NP_000153.1:p.Leu306=
NM_001354800.1:c.918G=	NP_001341729.1:p.Leu306=
NM_001354801.1:c.8+55G=	NP_001341730.1:n.8+55G=
NM_033507.2:c.921G=	NP_277042.1:p.Leu307=
NM_033508.2:c.915G=	NP_277043.1:p.Leu305=
NM_000162.5:c.918G= MANE Select	NP_000153.1:p.Leu306=
NM_033507.3:c.921G=	NP_277042.1:p.Leu307=
NM_033508.3:c.915G=	NP_277043.1:p.Leu305=