Canonical Allele Identifier: CA1703637076

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44152403C= , CM000669.2:g.44152403C=	GRCh38
NC_000007.13:g.44192002C= , CM000669.1:g.44192002C=	GRCh37
NC_000007.12:g.44158527C=	NCBI36
NG_008847.1:g.42021G=
NG_008847.2:g.50768G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*229G=	ENSP00000379142.4:n.*229G=
ENST00000616242.5:c.231G=	ENSP00000482149.2:p.Leu77=
ENST00000682635.1:n.717G=
ENST00000345378.7:c.234G=	ENSP00000223366.2:p.Leu78=
ENST00000403799.8:c.231G= MANE Select	ENSP00000384247.3:p.Leu77=
ENST00000671824.1:c.231G=	ENSP00000500264.1:p.Leu77=
ENST00000673284.1:c.231G=	ENSP00000499852.1:p.Leu77=
ENST00000345378.6:c.234G=	ENSP00000223366.2:p.Leu78=
ENST00000395796.7:c.228G=	ENSP00000379142.3:p.Leu76=
ENST00000403799.7:c.231G=	ENSP00000384247.3:p.Leu77=
ENST00000437084.1:c.231G=	ENSP00000402840.1:p.Leu77=
ENST00000616242.4:c.228G=	ENSP00000482149.1:p.Leu76=
NM_000162.3:c.231G=	NP_000153.1:p.Leu77=
NM_033507.1:c.234G=	NP_277042.1:p.Leu78=
NM_033508.1:c.228G=	NP_277043.1:p.Leu76=
NM_000162.4:c.231G=	NP_000153.1:p.Leu77=
NM_001354800.1:c.231G=	NP_001341729.1:p.Leu77=
NM_033507.2:c.234G=	NP_277042.1:p.Leu78=
NM_033508.2:c.228G=	NP_277043.1:p.Leu76=
NM_000162.5:c.231G= MANE Select	NP_000153.1:p.Leu77=
NM_033507.3:c.234G=	NP_277042.1:p.Leu78=
NM_033508.3:c.228G=	NP_277043.1:p.Leu76=