Canonical Allele Identifier: CA1703635862

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149790C= , CM000669.2:g.44149790C=	GRCh38
NC_000007.13:g.44189389C= , CM000669.1:g.44189389C=	GRCh37
NC_000007.12:g.44155914C=	NCBI36
NG_008847.1:g.44634G=
NG_008847.2:g.53381G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*647G=	ENSP00000379142.4:n.*647G=
ENST00000616242.5:c.649G=	ENSP00000482149.2:p.Asp217=
ENST00000682635.1:n.1135G=
ENST00000345378.7:c.652G=	ENSP00000223366.2:p.Asp218=
ENST00000403799.8:c.649G= MANE Select	ENSP00000384247.3:p.Asp217=
ENST00000671824.1:c.649G=	ENSP00000500264.1:p.Asp217=
ENST00000673284.1:c.649G=	ENSP00000499852.1:p.Asp217=
ENST00000345378.6:c.652G=	ENSP00000223366.2:p.Asp218=
ENST00000395796.7:c.646G=	ENSP00000379142.3:p.Asp216=
ENST00000403799.7:c.649G=	ENSP00000384247.3:p.Asp217=
ENST00000437084.1:c.598G=	ENSP00000402840.1:p.Asp200=
ENST00000616242.4:c.646G=	ENSP00000482149.1:p.Asp216=
NM_000162.3:c.649G=	NP_000153.1:p.Asp217=
NM_033507.1:c.652G=	NP_277042.1:p.Asp218=
NM_033508.1:c.646G=	NP_277043.1:p.Asp216=
NM_000162.4:c.649G=	NP_000153.1:p.Asp217=
NM_001354800.1:c.649G=	NP_001341729.1:p.Asp217=
NM_033507.2:c.652G=	NP_277042.1:p.Asp218=
NM_033508.2:c.646G=	NP_277043.1:p.Asp216=
NM_000162.5:c.649G= MANE Select	NP_000153.1:p.Asp217=
NM_033507.3:c.652G=	NP_277042.1:p.Asp218=
NM_033508.3:c.646G=	NP_277043.1:p.Asp216=