Canonical Allele Identifier: CA1703635871

Gene: GCK

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149808T= , CM000669.2:g.44149808T=	GRCh38
NC_000007.13:g.44189407T= , CM000669.1:g.44189407T=	GRCh37
NC_000007.12:g.44155932T=	NCBI36
NG_008847.1:g.44616A=
NG_008847.2:g.53363A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*629A=	ENSP00000379142.4:n.*629A=
ENST00000616242.5:c.631A=	ENSP00000482149.2:p.Ile211=
ENST00000682635.1:n.1117A=
ENST00000345378.7:c.634A=	ENSP00000223366.2:p.Ile212=
ENST00000403799.8:c.631A= MANE Select	ENSP00000384247.3:p.Ile211=
ENST00000671824.1:c.631A=	ENSP00000500264.1:p.Ile211=
ENST00000673284.1:c.631A=	ENSP00000499852.1:p.Ile211=
ENST00000345378.6:c.634A=	ENSP00000223366.2:p.Ile212=
ENST00000395796.7:c.628A=	ENSP00000379142.3:p.Ile210=
ENST00000403799.7:c.631A=	ENSP00000384247.3:p.Ile211=
ENST00000437084.1:c.580A=	ENSP00000402840.1:p.Ile194=
ENST00000616242.4:c.628A=	ENSP00000482149.1:p.Ile210=
NM_000162.3:c.631A=	NP_000153.1:p.Ile211=
NM_033507.1:c.634A=	NP_277042.1:p.Ile212=
NM_033508.1:c.628A=	NP_277043.1:p.Ile210=
NM_000162.4:c.631A=	NP_000153.1:p.Ile211=
NM_001354800.1:c.631A=	NP_001341729.1:p.Ile211=
NM_033507.2:c.634A=	NP_277042.1:p.Ile212=
NM_033508.2:c.628A=	NP_277043.1:p.Ile210=
NM_000162.5:c.631A= MANE Select	NP_000153.1:p.Ile211=
NM_033507.3:c.634A=	NP_277042.1:p.Ile212=
NM_033508.3:c.628A=	NP_277043.1:p.Ile210=