Canonical Allele Identifier: CA1703612678

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145212G= , CM000669.2:g.44145212G=	GRCh38
NC_000007.13:g.44184811G= , CM000669.1:g.44184811G=	GRCh37
NC_000007.12:g.44151336G=	NCBI36
NG_008847.1:g.49212C=
NG_008847.2:g.57959C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1320C=	ENSP00000379142.4:n.*1320C=
ENST00000616242.5:c.*442C=	ENSP00000482149.2:n.*442C=
ENST00000683378.1:n.548C=
ENST00000336642.9:c.356C=	ENSP00000338009.5:p.Ser119=
ENST00000345378.7:c.1325C=	ENSP00000223366.2:p.Ser442=
ENST00000403799.8:c.1322C= MANE Select	ENSP00000384247.3:p.Ser441=
ENST00000671824.1:c.1385C=	ENSP00000500264.1:p.Ser462=
ENST00000672743.1:n.334C=
ENST00000673284.1:c.1322C=	ENSP00000499852.1:p.Ser441=
ENST00000336642.8:c.374C=	ENSP00000338009.4:p.Ser125=
ENST00000345378.6:c.1325C=	ENSP00000223366.2:p.Ser442=
ENST00000395796.7:c.1319C=	ENSP00000379142.3:p.Ser440=
ENST00000403799.7:c.1322C=	ENSP00000384247.3:p.Ser441=
ENST00000437084.1:c.1271C=	ENSP00000402840.1:p.Ser424=
ENST00000459642.1:n.702C=
ENST00000616242.4:c.1319C=	ENSP00000482149.1:p.Ser440=
NM_000162.3:c.1322C=	NP_000153.1:p.Ser441=
NM_033507.1:c.1325C=	NP_277042.1:p.Ser442=
NM_033508.1:c.1319C=	NP_277043.1:p.Ser440=
NM_000162.4:c.1322C=	NP_000153.1:p.Ser441=
NM_001354800.1:c.1322C=	NP_001341729.1:p.Ser441=
NM_001354801.1:c.311C=	NP_001341730.1:p.Ser104=
NM_001354802.1:c.182C=	NP_001341731.1:p.Ser61=
NM_001354803.1:c.356C=	NP_001341732.1:p.Ser119=
NM_033507.2:c.1325C=	NP_277042.1:p.Ser442=
NM_033508.2:c.1319C=	NP_277043.1:p.Ser440=
XM_024446707.1:c.182C=	XP_024302475.1:p.Ser61=
NM_000162.5:c.1322C= MANE Select	NP_000153.1:p.Ser441=
NM_033507.3:c.1325C=	NP_277042.1:p.Ser442=
NM_033508.3:c.1319C=	NP_277043.1:p.Ser440=
NM_001354803.2:c.356C=	NP_001341732.1:p.Ser119=