Canonical Allele Identifier: CA1703612664

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145188G= , CM000669.2:g.44145188G=	GRCh38
NC_000007.13:g.44184787G= , CM000669.1:g.44184787G=	GRCh37
NC_000007.12:g.44151312G=	NCBI36
NG_008847.1:g.49236C=
NG_008847.2:g.57983C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1344C=	ENSP00000379142.4:n.*1344C=
ENST00000616242.5:c.*466C=	ENSP00000482149.2:n.*466C=
ENST00000683378.1:n.572C=
ENST00000336642.9:c.380C=	ENSP00000338009.5:p.Ala127=
ENST00000345378.7:c.1349C=	ENSP00000223366.2:p.Ala450=
ENST00000403799.8:c.1346C= MANE Select	ENSP00000384247.3:p.Ala449=
ENST00000671824.1:c.1409C=	ENSP00000500264.1:p.Ala470=
ENST00000672743.1:n.358C=
ENST00000673284.1:c.1346C=	ENSP00000499852.1:p.Ala449=
ENST00000336642.8:c.398C=	ENSP00000338009.4:p.Ala133=
ENST00000345378.6:c.1349C=	ENSP00000223366.2:p.Ala450=
ENST00000395796.7:c.1343C=	ENSP00000379142.3:p.Ala448=
ENST00000403799.7:c.1346C=	ENSP00000384247.3:p.Ala449=
ENST00000437084.1:c.1295C=	ENSP00000402840.1:p.Ala432=
ENST00000459642.1:n.726C=
ENST00000616242.4:c.1343C=	ENSP00000482149.1:p.Ala448=
NM_000162.3:c.1346C=	NP_000153.1:p.Ala449=
NM_033507.1:c.1349C=	NP_277042.1:p.Ala450=
NM_033508.1:c.1343C=	NP_277043.1:p.Ala448=
NM_000162.4:c.1346C=	NP_000153.1:p.Ala449=
NM_001354800.1:c.1346C=	NP_001341729.1:p.Ala449=
NM_001354801.1:c.335C=	NP_001341730.1:p.Ala112=
NM_001354802.1:c.206C=	NP_001341731.1:p.Ala69=
NM_001354803.1:c.380C=	NP_001341732.1:p.Ala127=
NM_033507.2:c.1349C=	NP_277042.1:p.Ala450=
NM_033508.2:c.1343C=	NP_277043.1:p.Ala448=
XM_024446707.1:c.206C=	XP_024302475.1:p.Ala69=
NM_000162.5:c.1346C= MANE Select	NP_000153.1:p.Ala449=
NM_033507.3:c.1349C=	NP_277042.1:p.Ala450=
NM_033508.3:c.1343C=	NP_277043.1:p.Ala448=
NM_001354803.2:c.380C=	NP_001341732.1:p.Ala127=