Canonical Allele Identifier: CA1703613454
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44146465C= , CM000669.2:g.44146465C= GRCh38
NC_000007.13:g.44186064C= , CM000669.1:g.44186064C= GRCh37
NC_000007.12:g.44152589C= NCBI36
NG_008847.1:g.47959G=
NG_008847.2:g.56706G=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*1015G= ENSP00000379142.4:n.*1015G=
ENST00000616242.5:c.*137G= ENSP00000482149.2:n.*137G=
ENST00000683378.1:n.243G=
ENST00000345378.7:c.1020G= ENSP00000223366.2:p.Glu340=
ENST00000403799.8:c.1017G= MANE Select ENSP00000384247.3:p.Glu339=
ENST00000671824.1:c.1080G= ENSP00000500264.1:p.Glu360=
ENST00000673284.1:c.1017G= ENSP00000499852.1:p.Glu339=
ENST00000345378.6:c.1020G= ENSP00000223366.2:p.Glu340=
ENST00000395796.7:c.1014G= ENSP00000379142.3:p.Glu338=
ENST00000403799.7:c.1017G= ENSP00000384247.3:p.Glu339=
ENST00000437084.1:c.966G= ENSP00000402840.1:p.Glu322=
ENST00000473353.1:n.315G=
ENST00000616242.4:c.1014G= ENSP00000482149.1:p.Glu338=
NM_000162.3:c.1017G= NP_000153.1:p.Glu339=
NM_033507.1:c.1020G= NP_277042.1:p.Glu340=
NM_033508.1:c.1014G= NP_277043.1:p.Glu338=
NM_000162.4:c.1017G= NP_000153.1:p.Glu339=
NM_001354800.1:c.1017G= NP_001341729.1:p.Glu339=
NM_001354801.1:c.8+154G= NP_001341730.1:n.8+154G=
NM_033507.2:c.1020G= NP_277042.1:p.Glu340=
NM_033508.2:c.1014G= NP_277043.1:p.Glu338=
NM_000162.5:c.1017G= MANE Select NP_000153.1:p.Glu339=
NM_033507.3:c.1020G= NP_277042.1:p.Glu340=
NM_033508.3:c.1014G= NP_277043.1:p.Glu338=