Canonical Allele Identifier: CA1703612938

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145644C= , CM000669.2:g.44145644C=	GRCh38
NC_000007.13:g.44185243C= , CM000669.1:g.44185243C=	GRCh37
NC_000007.12:g.44151768C=	NCBI36
NG_008847.1:g.48780G=
NG_008847.2:g.57527G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1104G=	ENSP00000379142.4:n.*1104G=
ENST00000616242.5:c.*226G=	ENSP00000482149.2:n.*226G=
ENST00000683378.1:n.332G=
ENST00000336642.9:c.140G=	ENSP00000338009.5:p.Arg47=
ENST00000345378.7:c.1109G=	ENSP00000223366.2:p.Arg370=
ENST00000403799.8:c.1106G= MANE Select	ENSP00000384247.3:p.Arg369=
ENST00000671824.1:c.1169G=	ENSP00000500264.1:p.Arg390=
ENST00000672743.1:n.118G=
ENST00000673284.1:c.1106G=	ENSP00000499852.1:p.Arg369=
ENST00000336642.8:c.158G=	ENSP00000338009.4:p.Arg53=
ENST00000345378.6:c.1109G=	ENSP00000223366.2:p.Arg370=
ENST00000395796.7:c.1103G=	ENSP00000379142.3:p.Arg368=
ENST00000403799.7:c.1106G=	ENSP00000384247.3:p.Arg369=
ENST00000437084.1:c.1055G=	ENSP00000402840.1:p.Arg352=
ENST00000459642.1:n.486G=
ENST00000473353.1:n.404G=
ENST00000616242.4:c.1103G=	ENSP00000482149.1:p.Arg368=
NM_000162.3:c.1106G=	NP_000153.1:p.Arg369=
NM_033507.1:c.1109G=	NP_277042.1:p.Arg370=
NM_033508.1:c.1103G=	NP_277043.1:p.Arg368=
NM_000162.4:c.1106G=	NP_000153.1:p.Arg369=
NM_001354800.1:c.1106G=	NP_001341729.1:p.Arg369=
NM_001354801.1:c.95G=	NP_001341730.1:p.Arg32=
NM_001354802.1:c.-35G=	NP_001341731.1:n.-35G=
NM_001354803.1:c.140G=	NP_001341732.1:p.Arg47=
NM_033507.2:c.1109G=	NP_277042.1:p.Arg370=
NM_033508.2:c.1103G=	NP_277043.1:p.Arg368=
XM_024446707.1:c.-35G=	XP_024302475.1:n.-35G=
NM_000162.5:c.1106G= MANE Select	NP_000153.1:p.Arg369=
NM_033507.3:c.1109G=	NP_277042.1:p.Arg370=
NM_033508.3:c.1103G=	NP_277043.1:p.Arg368=
NM_001354803.2:c.140G=	NP_001341732.1:p.Arg47=