Canonical Allele Identifier: CA1703637569

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153411A= , CM000669.2:g.44153411A=	GRCh38
NC_000007.13:g.44193010A= , CM000669.1:g.44193010A=	GRCh37
NC_000007.12:g.44159535A=	NCBI36
NG_008847.1:g.41013T=
NG_008847.2:g.49760T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*96T=	ENSP00000379142.4:n.*96T=
ENST00000616242.5:c.98T=	ENSP00000482149.2:p.Val33=
ENST00000682635.1:n.584T=
ENST00000345378.7:c.101T=	ENSP00000223366.2:p.Val34=
ENST00000403799.8:c.98T= MANE Select	ENSP00000384247.3:p.Val33=
ENST00000671824.1:c.98T=	ENSP00000500264.1:p.Val33=
ENST00000673284.1:c.98T=	ENSP00000499852.1:p.Val33=
ENST00000345378.6:c.101T=	ENSP00000223366.2:p.Val34=
ENST00000395796.7:c.95T=	ENSP00000379142.3:p.Val32=
ENST00000403799.7:c.98T=	ENSP00000384247.3:p.Val33=
ENST00000437084.1:c.98T=	ENSP00000402840.1:p.Val33=
ENST00000476008.1:n.533T=
ENST00000616242.4:c.95T=	ENSP00000482149.1:p.Val32=
NM_000162.3:c.98T=	NP_000153.1:p.Val33=
NM_033507.1:c.101T=	NP_277042.1:p.Val34=
NM_033508.1:c.95T=	NP_277043.1:p.Val32=
NM_000162.4:c.98T=	NP_000153.1:p.Val33=
NM_001354800.1:c.98T=	NP_001341729.1:p.Val33=
NM_033507.2:c.101T=	NP_277042.1:p.Val34=
NM_033508.2:c.95T=	NP_277043.1:p.Val32=
NM_000162.5:c.98T= MANE Select	NP_000153.1:p.Val33=
NM_033507.3:c.101T=	NP_277042.1:p.Val34=
NM_033508.3:c.95T=	NP_277043.1:p.Val32=