Canonical Allele Identifier: CA1703635997

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44150057A= , CM000669.2:g.44150057A=	GRCh38
NC_000007.13:g.44189656A= , CM000669.1:g.44189656A=	GRCh37
NC_000007.12:g.44156181A=	NCBI36
NG_008847.1:g.44367T=
NG_008847.2:g.53114T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*489T=	ENSP00000379142.4:n.*489T=
ENST00000616242.5:c.491T=	ENSP00000482149.2:p.Leu164=
ENST00000682635.1:n.977T=
ENST00000345378.7:c.494T=	ENSP00000223366.2:p.Leu165=
ENST00000403799.8:c.491T= MANE Select	ENSP00000384247.3:p.Leu164=
ENST00000671824.1:c.491T=	ENSP00000500264.1:p.Leu164=
ENST00000673284.1:c.491T=	ENSP00000499852.1:p.Leu164=
ENST00000345378.6:c.494T=	ENSP00000223366.2:p.Leu165=
ENST00000395796.7:c.488T=	ENSP00000379142.3:p.Leu163=
ENST00000403799.7:c.491T=	ENSP00000384247.3:p.Leu164=
ENST00000437084.1:c.440T=	ENSP00000402840.1:p.Leu147=
ENST00000616242.4:c.488T=	ENSP00000482149.1:p.Leu163=
NM_000162.3:c.491T=	NP_000153.1:p.Leu164=
NM_033507.1:c.494T=	NP_277042.1:p.Leu165=
NM_033508.1:c.488T=	NP_277043.1:p.Leu163=
NM_000162.4:c.491T=	NP_000153.1:p.Leu164=
NM_001354800.1:c.491T=	NP_001341729.1:p.Leu164=
NM_033507.2:c.494T=	NP_277042.1:p.Leu165=
NM_033508.2:c.488T=	NP_277043.1:p.Leu163=
NM_000162.5:c.491T= MANE Select	NP_000153.1:p.Leu164=
NM_033507.3:c.494T=	NP_277042.1:p.Leu165=
NM_033508.3:c.488T=	NP_277043.1:p.Leu163=