Canonical Allele Identifier: CA1703634885

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147685C= , CM000669.2:g.44147685C=	GRCh38
NC_000007.13:g.44187284C= , CM000669.1:g.44187284C=	GRCh37
NC_000007.12:g.44153809C=	NCBI36
NG_008847.1:g.46739G=
NG_008847.2:g.55486G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*826G=	ENSP00000379142.4:n.*826G=
ENST00000616242.5:c.828G=	ENSP00000482149.2:p.Leu276=
ENST00000345378.7:c.831G=	ENSP00000223366.2:p.Leu277=
ENST00000403799.8:c.828G= MANE Select	ENSP00000384247.3:p.Leu276=
ENST00000671824.1:c.828G=	ENSP00000500264.1:p.Leu276=
ENST00000673284.1:c.828G=	ENSP00000499852.1:p.Leu276=
ENST00000345378.6:c.831G=	ENSP00000223366.2:p.Leu277=
ENST00000395796.7:c.825G=	ENSP00000379142.3:p.Leu275=
ENST00000403799.7:c.828G=	ENSP00000384247.3:p.Leu276=
ENST00000437084.1:c.777G=	ENSP00000402840.1:p.Leu259=
ENST00000616242.4:c.825G=	ENSP00000482149.1:p.Leu275=
NM_000162.3:c.828G=	NP_000153.1:p.Leu276=
NM_033507.1:c.831G=	NP_277042.1:p.Leu277=
NM_033508.1:c.825G=	NP_277043.1:p.Leu275=
XR_927223.1:n.19C=
NM_000162.4:c.828G=	NP_000153.1:p.Leu276=
NM_001354800.1:c.828G=	NP_001341729.1:p.Leu276=
NM_033507.2:c.831G=	NP_277042.1:p.Leu277=
NM_033508.2:c.825G=	NP_277043.1:p.Leu275=
XR_927223.2:n.19C=
NM_000162.5:c.828G= MANE Select	NP_000153.1:p.Leu276=
NM_033507.3:c.831G=	NP_277042.1:p.Leu277=
NM_033508.3:c.825G=	NP_277043.1:p.Leu275=