Canonical Allele Identifier: CA1703634900
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147711C= , CM000669.2:g.44147711C= GRCh38
NC_000007.13:g.44187310C= , CM000669.1:g.44187310C= GRCh37
NC_000007.12:g.44153835C= NCBI36
NG_008847.1:g.46713G=
NG_008847.2:g.55460G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*800G= ENSP00000379142.4:n.*800G=
ENST00000616242.5:c.802G= ENSP00000482149.2:p.Glu268=
ENST00000345378.7:c.805G= ENSP00000223366.2:p.Glu269=
ENST00000403799.8:c.802G= MANE Select ENSP00000384247.3:p.Glu268=
ENST00000671824.1:c.802G= ENSP00000500264.1:p.Glu268=
ENST00000673284.1:c.802G= ENSP00000499852.1:p.Glu268=
ENST00000345378.6:c.805G= ENSP00000223366.2:p.Glu269=
ENST00000395796.7:c.799G= ENSP00000379142.3:p.Glu267=
ENST00000403799.7:c.802G= ENSP00000384247.3:p.Glu268=
ENST00000437084.1:c.751G= ENSP00000402840.1:p.Glu251=
ENST00000616242.4:c.799G= ENSP00000482149.1:p.Glu267=
NM_000162.3:c.802G= NP_000153.1:p.Glu268=
NM_033507.1:c.805G= NP_277042.1:p.Glu269=
NM_033508.1:c.799G= NP_277043.1:p.Glu267=
XR_927223.1:n.45C=
NM_000162.4:c.802G= NP_000153.1:p.Glu268=
NM_001354800.1:c.802G= NP_001341729.1:p.Glu268=
NM_033507.2:c.805G= NP_277042.1:p.Glu269=
NM_033508.2:c.799G= NP_277043.1:p.Glu267=
XR_927223.2:n.45C=
NM_000162.5:c.802G= MANE Select NP_000153.1:p.Glu268=
NM_033507.3:c.805G= NP_277042.1:p.Glu269=
NM_033508.3:c.799G= NP_277043.1:p.Glu267=