Canonical Allele Identifier: CA1703636439
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150970C= , CM000669.2:g.44150970C= GRCh38
NC_000007.13:g.44190569C= , CM000669.1:g.44190569C= GRCh37
NC_000007.12:g.44157094C= NCBI36
NG_008847.1:g.43454G=
NG_008847.2:g.52201G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*467G= ENSP00000379142.4:n.*467G=
ENST00000616242.5:c.469G= ENSP00000482149.2:p.Glu157=
ENST00000682635.1:n.955G=
ENST00000345378.7:c.472G= ENSP00000223366.2:p.Glu158=
ENST00000403799.8:c.469G= MANE Select ENSP00000384247.3:p.Glu157=
ENST00000671824.1:c.469G= ENSP00000500264.1:p.Glu157=
ENST00000673284.1:c.469G= ENSP00000499852.1:p.Glu157=
ENST00000345378.6:c.472G= ENSP00000223366.2:p.Glu158=
ENST00000395796.7:c.466G= ENSP00000379142.3:p.Glu156=
ENST00000403799.7:c.469G= ENSP00000384247.3:p.Glu157=
ENST00000437084.1:c.418G= ENSP00000402840.1:p.Glu140=
ENST00000616242.4:c.466G= ENSP00000482149.1:p.Glu156=
NM_000162.3:c.469G= NP_000153.1:p.Glu157=
NM_033507.1:c.472G= NP_277042.1:p.Glu158=
NM_033508.1:c.466G= NP_277043.1:p.Glu156=
NM_000162.4:c.469G= NP_000153.1:p.Glu157=
NM_001354800.1:c.469G= NP_001341729.1:p.Glu157=
NM_033507.2:c.472G= NP_277042.1:p.Glu158=
NM_033508.2:c.466G= NP_277043.1:p.Glu156=
NM_000162.5:c.469G= MANE Select NP_000153.1:p.Glu157=
NM_033507.3:c.472G= NP_277042.1:p.Glu158=
NM_033508.3:c.466G= NP_277043.1:p.Glu156=