Canonical Allele Identifier: CA1703612685

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145226G= , CM000669.2:g.44145226G=	GRCh38
NC_000007.13:g.44184825G= , CM000669.1:g.44184825G=	GRCh37
NC_000007.12:g.44151350G=	NCBI36
NG_008847.1:g.49198C=
NG_008847.2:g.57945C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1306C=	ENSP00000379142.4:n.*1306C=
ENST00000616242.5:c.*428C=	ENSP00000482149.2:n.*428C=
ENST00000683378.1:n.534C=
ENST00000336642.9:c.342C=	ENSP00000338009.5:p.Ile114=
ENST00000345378.7:c.1311C=	ENSP00000223366.2:p.Ile437=
ENST00000403799.8:c.1308C= MANE Select	ENSP00000384247.3:p.Ile436=
ENST00000671824.1:c.1371C=	ENSP00000500264.1:p.Ile457=
ENST00000672743.1:n.320C=
ENST00000673284.1:c.1308C=	ENSP00000499852.1:p.Ile436=
ENST00000336642.8:c.360C=	ENSP00000338009.4:p.Ile120=
ENST00000345378.6:c.1311C=	ENSP00000223366.2:p.Ile437=
ENST00000395796.7:c.1305C=	ENSP00000379142.3:p.Ile435=
ENST00000403799.7:c.1308C=	ENSP00000384247.3:p.Ile436=
ENST00000437084.1:c.1257C=	ENSP00000402840.1:p.Ile419=
ENST00000459642.1:n.688C=
ENST00000616242.4:c.1305C=	ENSP00000482149.1:p.Ile435=
NM_000162.3:c.1308C=	NP_000153.1:p.Ile436=
NM_033507.1:c.1311C=	NP_277042.1:p.Ile437=
NM_033508.1:c.1305C=	NP_277043.1:p.Ile435=
NM_000162.4:c.1308C=	NP_000153.1:p.Ile436=
NM_001354800.1:c.1308C=	NP_001341729.1:p.Ile436=
NM_001354801.1:c.297C=	NP_001341730.1:p.Ile99=
NM_001354802.1:c.168C=	NP_001341731.1:p.Ile56=
NM_001354803.1:c.342C=	NP_001341732.1:p.Ile114=
NM_033507.2:c.1311C=	NP_277042.1:p.Ile437=
NM_033508.2:c.1305C=	NP_277043.1:p.Ile435=
XM_024446707.1:c.168C=	XP_024302475.1:p.Ile56=
NM_000162.5:c.1308C= MANE Select	NP_000153.1:p.Ile436=
NM_033507.3:c.1311C=	NP_277042.1:p.Ile437=
NM_033508.3:c.1305C=	NP_277043.1:p.Ile435=
NM_001354803.2:c.342C=	NP_001341732.1:p.Ile114=