Canonical Allele Identifier: CA1703613467

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146492G= , CM000669.2:g.44146492G=	GRCh38
NC_000007.13:g.44186091G= , CM000669.1:g.44186091G=	GRCh37
NC_000007.12:g.44152616G=	NCBI36
NG_008847.1:g.47932C=
NG_008847.2:g.56679C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*988C=	ENSP00000379142.4:n.*988C=
ENST00000616242.5:c.*110C=	ENSP00000482149.2:n.*110C=
ENST00000683378.1:n.216C=
ENST00000345378.7:c.993C=	ENSP00000223366.2:p.Phe331=
ENST00000403799.8:c.990C= MANE Select	ENSP00000384247.3:p.Phe330=
ENST00000671824.1:c.1053C=	ENSP00000500264.1:p.Phe351=
ENST00000673284.1:c.990C=	ENSP00000499852.1:p.Phe330=
ENST00000345378.6:c.993C=	ENSP00000223366.2:p.Phe331=
ENST00000395796.7:c.987C=	ENSP00000379142.3:p.Phe329=
ENST00000403799.7:c.990C=	ENSP00000384247.3:p.Phe330=
ENST00000437084.1:c.939C=	ENSP00000402840.1:p.Phe313=
ENST00000473353.1:n.288C=
ENST00000616242.4:c.987C=	ENSP00000482149.1:p.Phe329=
NM_000162.3:c.990C=	NP_000153.1:p.Phe330=
NM_033507.1:c.993C=	NP_277042.1:p.Phe331=
NM_033508.1:c.987C=	NP_277043.1:p.Phe329=
NM_000162.4:c.990C=	NP_000153.1:p.Phe330=
NM_001354800.1:c.990C=	NP_001341729.1:p.Phe330=
NM_001354801.1:c.8+127C=	NP_001341730.1:n.8+127C=
NM_033507.2:c.993C=	NP_277042.1:p.Phe331=
NM_033508.2:c.987C=	NP_277043.1:p.Phe329=
NM_000162.5:c.990C= MANE Select	NP_000153.1:p.Phe330=
NM_033507.3:c.993C=	NP_277042.1:p.Phe331=
NM_033508.3:c.987C=	NP_277043.1:p.Phe329=