Canonical Allele Identifier: CA1703612703

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145253C= , CM000669.2:g.44145253C=	GRCh38
NC_000007.13:g.44184852C= , CM000669.1:g.44184852C=	GRCh37
NC_000007.12:g.44151377C=	NCBI36
NG_008847.1:g.49171G=
NG_008847.2:g.57918G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1279G=	ENSP00000379142.4:n.*1279G=
ENST00000616242.5:c.*401G=	ENSP00000482149.2:n.*401G=
ENST00000683378.1:n.507G=
ENST00000336642.9:c.315G=	ENSP00000338009.5:p.Val105=
ENST00000345378.7:c.1284G=	ENSP00000223366.2:p.Val428=
ENST00000403799.8:c.1281G= MANE Select	ENSP00000384247.3:p.Val427=
ENST00000671824.1:c.1344G=	ENSP00000500264.1:p.Val448=
ENST00000672743.1:n.293G=
ENST00000673284.1:c.1281G=	ENSP00000499852.1:p.Val427=
ENST00000336642.8:c.333G=	ENSP00000338009.4:p.Val111=
ENST00000345378.6:c.1284G=	ENSP00000223366.2:p.Val428=
ENST00000395796.7:c.1278G=	ENSP00000379142.3:p.Val426=
ENST00000403799.7:c.1281G=	ENSP00000384247.3:p.Val427=
ENST00000437084.1:c.1230G=	ENSP00000402840.1:p.Val410=
ENST00000459642.1:n.661G=
ENST00000616242.4:c.1278G=	ENSP00000482149.1:p.Val426=
NM_000162.3:c.1281G=	NP_000153.1:p.Val427=
NM_033507.1:c.1284G=	NP_277042.1:p.Val428=
NM_033508.1:c.1278G=	NP_277043.1:p.Val426=
NM_000162.4:c.1281G=	NP_000153.1:p.Val427=
NM_001354800.1:c.1281G=	NP_001341729.1:p.Val427=
NM_001354801.1:c.270G=	NP_001341730.1:p.Val90=
NM_001354802.1:c.141G=	NP_001341731.1:p.Val47=
NM_001354803.1:c.315G=	NP_001341732.1:p.Val105=
NM_033507.2:c.1284G=	NP_277042.1:p.Val428=
NM_033508.2:c.1278G=	NP_277043.1:p.Val426=
XM_024446707.1:c.141G=	XP_024302475.1:p.Val47=
NM_000162.5:c.1281G= MANE Select	NP_000153.1:p.Val427=
NM_033507.3:c.1284G=	NP_277042.1:p.Val428=
NM_033508.3:c.1278G=	NP_277043.1:p.Val426=
NM_001354803.2:c.315G=	NP_001341732.1:p.Val105=