Canonical Allele Identifier: CA1703637572

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153420A= , CM000669.2:g.44153420A=	GRCh38
NC_000007.13:g.44193019A= , CM000669.1:g.44193019A=	GRCh37
NC_000007.12:g.44159544A=	NCBI36
NG_008847.1:g.41004T=
NG_008847.2:g.49751T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*87T=	ENSP00000379142.4:n.*87T=
ENST00000616242.5:c.89T=	ENSP00000482149.2:p.Leu30=
ENST00000682635.1:n.575T=
ENST00000345378.7:c.92T=	ENSP00000223366.2:p.Leu31=
ENST00000403799.8:c.89T= MANE Select	ENSP00000384247.3:p.Leu30=
ENST00000671824.1:c.89T=	ENSP00000500264.1:p.Leu30=
ENST00000673284.1:c.89T=	ENSP00000499852.1:p.Leu30=
ENST00000345378.6:c.92T=	ENSP00000223366.2:p.Leu31=
ENST00000395796.7:c.86T=	ENSP00000379142.3:p.Leu29=
ENST00000403799.7:c.89T=	ENSP00000384247.3:p.Leu30=
ENST00000437084.1:c.89T=	ENSP00000402840.1:p.Leu30=
ENST00000476008.1:n.524T=
ENST00000616242.4:c.86T=	ENSP00000482149.1:p.Leu29=
NM_000162.3:c.89T=	NP_000153.1:p.Leu30=
NM_033507.1:c.92T=	NP_277042.1:p.Leu31=
NM_033508.1:c.86T=	NP_277043.1:p.Leu29=
NM_000162.4:c.89T=	NP_000153.1:p.Leu30=
NM_001354800.1:c.89T=	NP_001341729.1:p.Leu30=
NM_033507.2:c.92T=	NP_277042.1:p.Leu31=
NM_033508.2:c.86T=	NP_277043.1:p.Leu29=
NM_000162.5:c.89T= MANE Select	NP_000153.1:p.Leu30=
NM_033507.3:c.92T=	NP_277042.1:p.Leu31=
NM_033508.3:c.86T=	NP_277043.1:p.Leu29=