Canonical Allele Identifier: CA1703613453

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146464T= , CM000669.2:g.44146464T=	GRCh38
NC_000007.13:g.44186063T= , CM000669.1:g.44186063T=	GRCh37
NC_000007.12:g.44152588T=	NCBI36
NG_008847.1:g.47960A=
NG_008847.2:g.56707A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1016A=	ENSP00000379142.4:n.*1016A=
ENST00000616242.5:c.*138A=	ENSP00000482149.2:n.*138A=
ENST00000683378.1:n.244A=
ENST00000345378.7:c.1021A=	ENSP00000223366.2:p.Ser341=
ENST00000403799.8:c.1018A= MANE Select	ENSP00000384247.3:p.Ser340=
ENST00000671824.1:c.1081A=	ENSP00000500264.1:p.Ser361=
ENST00000673284.1:c.1018A=	ENSP00000499852.1:p.Ser340=
ENST00000345378.6:c.1021A=	ENSP00000223366.2:p.Ser341=
ENST00000395796.7:c.1015A=	ENSP00000379142.3:p.Ser339=
ENST00000403799.7:c.1018A=	ENSP00000384247.3:p.Ser340=
ENST00000437084.1:c.967A=	ENSP00000402840.1:p.Ser323=
ENST00000473353.1:n.316A=
ENST00000616242.4:c.1015A=	ENSP00000482149.1:p.Ser339=
NM_000162.3:c.1018A=	NP_000153.1:p.Ser340=
NM_033507.1:c.1021A=	NP_277042.1:p.Ser341=
NM_033508.1:c.1015A=	NP_277043.1:p.Ser339=
NM_000162.4:c.1018A=	NP_000153.1:p.Ser340=
NM_001354800.1:c.1018A=	NP_001341729.1:p.Ser340=
NM_001354801.1:c.8+155A=	NP_001341730.1:n.8+155A=
NM_033507.2:c.1021A=	NP_277042.1:p.Ser341=
NM_033508.2:c.1015A=	NP_277043.1:p.Ser339=
NM_000162.5:c.1018A= MANE Select	NP_000153.1:p.Ser340=
NM_033507.3:c.1021A=	NP_277042.1:p.Ser341=
NM_033508.3:c.1015A=	NP_277043.1:p.Ser339=