Canonical Allele Identifier: CA1703613485

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146534G= , CM000669.2:g.44146534G=	GRCh38
NC_000007.13:g.44186133G= , CM000669.1:g.44186133G=	GRCh37
NC_000007.12:g.44152658G=	NCBI36
NG_008847.1:g.47890C=
NG_008847.2:g.56637C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*946C=	ENSP00000379142.4:n.*946C=
ENST00000616242.5:c.*68C=	ENSP00000482149.2:n.*68C=
ENST00000683378.1:n.174C=
ENST00000345378.7:c.951C=	ENSP00000223366.2:p.Phe317=
ENST00000403799.8:c.948C= MANE Select	ENSP00000384247.3:p.Phe316=
ENST00000671824.1:c.1011C=	ENSP00000500264.1:p.Phe337=
ENST00000673284.1:c.948C=	ENSP00000499852.1:p.Phe316=
ENST00000345378.6:c.951C=	ENSP00000223366.2:p.Phe317=
ENST00000395796.7:c.945C=	ENSP00000379142.3:p.Phe315=
ENST00000403799.7:c.948C=	ENSP00000384247.3:p.Phe316=
ENST00000437084.1:c.897C=	ENSP00000402840.1:p.Phe299=
ENST00000473353.1:n.246C=
ENST00000616242.4:c.945C=	ENSP00000482149.1:p.Phe315=
NM_000162.3:c.948C=	NP_000153.1:p.Phe316=
NM_033507.1:c.951C=	NP_277042.1:p.Phe317=
NM_033508.1:c.945C=	NP_277043.1:p.Phe315=
NM_000162.4:c.948C=	NP_000153.1:p.Phe316=
NM_001354800.1:c.948C=	NP_001341729.1:p.Phe316=
NM_001354801.1:c.8+85C=	NP_001341730.1:n.8+85C=
NM_033507.2:c.951C=	NP_277042.1:p.Phe317=
NM_033508.2:c.945C=	NP_277043.1:p.Phe315=
NM_000162.5:c.948C= MANE Select	NP_000153.1:p.Phe316=
NM_033507.3:c.951C=	NP_277042.1:p.Phe317=
NM_033508.3:c.945C=	NP_277043.1:p.Phe315=