Canonical Allele Identifier: CA1703612713

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145272T= , CM000669.2:g.44145272T=	GRCh38
NC_000007.13:g.44184871T= , CM000669.1:g.44184871T=	GRCh37
NC_000007.12:g.44151396T=	NCBI36
NG_008847.1:g.49152A=
NG_008847.2:g.57899A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1260A=	ENSP00000379142.4:n.*1260A=
ENST00000616242.5:c.*382A=	ENSP00000482149.2:n.*382A=
ENST00000683378.1:n.488A=
ENST00000336642.9:c.296A=	ENSP00000338009.5:p.Glu99=
ENST00000345378.7:c.1265A=	ENSP00000223366.2:p.Glu422=
ENST00000403799.8:c.1262A= MANE Select	ENSP00000384247.3:p.Glu421=
ENST00000671824.1:c.1325A=	ENSP00000500264.1:p.Glu442=
ENST00000672743.1:n.274A=
ENST00000673284.1:c.1262A=	ENSP00000499852.1:p.Glu421=
ENST00000336642.8:c.314A=	ENSP00000338009.4:p.Glu105=
ENST00000345378.6:c.1265A=	ENSP00000223366.2:p.Glu422=
ENST00000395796.7:c.1259A=	ENSP00000379142.3:p.Glu420=
ENST00000403799.7:c.1262A=	ENSP00000384247.3:p.Glu421=
ENST00000437084.1:c.1211A=	ENSP00000402840.1:p.Glu404=
ENST00000459642.1:n.642A=
ENST00000616242.4:c.1259A=	ENSP00000482149.1:p.Glu420=
NM_000162.3:c.1262A=	NP_000153.1:p.Glu421=
NM_033507.1:c.1265A=	NP_277042.1:p.Glu422=
NM_033508.1:c.1259A=	NP_277043.1:p.Glu420=
NM_000162.4:c.1262A=	NP_000153.1:p.Glu421=
NM_001354800.1:c.1262A=	NP_001341729.1:p.Glu421=
NM_001354801.1:c.251A=	NP_001341730.1:p.Glu84=
NM_001354802.1:c.122A=	NP_001341731.1:p.Glu41=
NM_001354803.1:c.296A=	NP_001341732.1:p.Glu99=
NM_033507.2:c.1265A=	NP_277042.1:p.Glu422=
NM_033508.2:c.1259A=	NP_277043.1:p.Glu420=
XM_024446707.1:c.122A=	XP_024302475.1:p.Glu41=
NM_000162.5:c.1262A= MANE Select	NP_000153.1:p.Glu421=
NM_033507.3:c.1265A=	NP_277042.1:p.Glu422=
NM_033508.3:c.1259A=	NP_277043.1:p.Glu420=
NM_001354803.2:c.296A=	NP_001341732.1:p.Glu99=