Canonical Allele Identifier: CA1703612675

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145207C= , CM000669.2:g.44145207C=	GRCh38
NC_000007.13:g.44184806C= , CM000669.1:g.44184806C=	GRCh37
NC_000007.12:g.44151331C=	NCBI36
NG_008847.1:g.49217G=
NG_008847.2:g.57964G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1325G=	ENSP00000379142.4:n.*1325G=
ENST00000616242.5:c.*447G=	ENSP00000482149.2:n.*447G=
ENST00000683378.1:n.553G=
ENST00000336642.9:c.361G=	ENSP00000338009.5:p.Glu121=
ENST00000345378.7:c.1330G=	ENSP00000223366.2:p.Glu444=
ENST00000403799.8:c.1327G= MANE Select	ENSP00000384247.3:p.Glu443=
ENST00000671824.1:c.1390G=	ENSP00000500264.1:p.Glu464=
ENST00000672743.1:n.339G=
ENST00000673284.1:c.1327G=	ENSP00000499852.1:p.Glu443=
ENST00000336642.8:c.379G=	ENSP00000338009.4:p.Glu127=
ENST00000345378.6:c.1330G=	ENSP00000223366.2:p.Glu444=
ENST00000395796.7:c.1324G=	ENSP00000379142.3:p.Glu442=
ENST00000403799.7:c.1327G=	ENSP00000384247.3:p.Glu443=
ENST00000437084.1:c.1276G=	ENSP00000402840.1:p.Glu426=
ENST00000459642.1:n.707G=
ENST00000616242.4:c.1324G=	ENSP00000482149.1:p.Glu442=
NM_000162.3:c.1327G=	NP_000153.1:p.Glu443=
NM_033507.1:c.1330G=	NP_277042.1:p.Glu444=
NM_033508.1:c.1324G=	NP_277043.1:p.Glu442=
NM_000162.4:c.1327G=	NP_000153.1:p.Glu443=
NM_001354800.1:c.1327G=	NP_001341729.1:p.Glu443=
NM_001354801.1:c.316G=	NP_001341730.1:p.Glu106=
NM_001354802.1:c.187G=	NP_001341731.1:p.Glu63=
NM_001354803.1:c.361G=	NP_001341732.1:p.Glu121=
NM_033507.2:c.1330G=	NP_277042.1:p.Glu444=
NM_033508.2:c.1324G=	NP_277043.1:p.Glu442=
XM_024446707.1:c.187G=	XP_024302475.1:p.Glu63=
NM_000162.5:c.1327G= MANE Select	NP_000153.1:p.Glu443=
NM_033507.3:c.1330G=	NP_277042.1:p.Glu444=
NM_033508.3:c.1324G=	NP_277043.1:p.Glu442=
NM_001354803.2:c.361G=	NP_001341732.1:p.Glu121=