Canonical Allele Identifier: CA1703613476

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146511A= , CM000669.2:g.44146511A=	GRCh38
NC_000007.13:g.44186110A= , CM000669.1:g.44186110A=	GRCh37
NC_000007.12:g.44152635A=	NCBI36
NG_008847.1:g.47913T=
NG_008847.2:g.56660T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*969T=	ENSP00000379142.4:n.*969T=
ENST00000616242.5:c.*91T=	ENSP00000482149.2:n.*91T=
ENST00000683378.1:n.197T=
ENST00000345378.7:c.974T=	ENSP00000223366.2:p.Leu325=
ENST00000403799.8:c.971T= MANE Select	ENSP00000384247.3:p.Leu324=
ENST00000671824.1:c.1034T=	ENSP00000500264.1:p.Leu345=
ENST00000673284.1:c.971T=	ENSP00000499852.1:p.Leu324=
ENST00000345378.6:c.974T=	ENSP00000223366.2:p.Leu325=
ENST00000395796.7:c.968T=	ENSP00000379142.3:p.Leu323=
ENST00000403799.7:c.971T=	ENSP00000384247.3:p.Leu324=
ENST00000437084.1:c.920T=	ENSP00000402840.1:p.Leu307=
ENST00000473353.1:n.269T=
ENST00000616242.4:c.968T=	ENSP00000482149.1:p.Leu323=
NM_000162.3:c.971T=	NP_000153.1:p.Leu324=
NM_033507.1:c.974T=	NP_277042.1:p.Leu325=
NM_033508.1:c.968T=	NP_277043.1:p.Leu323=
NM_000162.4:c.971T=	NP_000153.1:p.Leu324=
NM_001354800.1:c.971T=	NP_001341729.1:p.Leu324=
NM_001354801.1:c.8+108T=	NP_001341730.1:n.8+108T=
NM_033507.2:c.974T=	NP_277042.1:p.Leu325=
NM_033508.2:c.968T=	NP_277043.1:p.Leu323=
NM_000162.5:c.971T= MANE Select	NP_000153.1:p.Leu324=
NM_033507.3:c.974T=	NP_277042.1:p.Leu325=
NM_033508.3:c.968T=	NP_277043.1:p.Leu323=