Canonical Allele Identifier: CA1703634927
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147757G= , CM000669.2:g.44147757G= GRCh38
NC_000007.13:g.44187356G= , CM000669.1:g.44187356G= GRCh37
NC_000007.12:g.44153881G= NCBI36
NG_008847.1:g.46667C=
NG_008847.2:g.55414C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*754C= ENSP00000379142.4:n.*754C=
ENST00000616242.5:c.756C= ENSP00000482149.2:p.Cys252=
ENST00000345378.7:c.759C= ENSP00000223366.2:p.Cys253=
ENST00000403799.8:c.756C= MANE Select ENSP00000384247.3:p.Cys252=
ENST00000671824.1:c.756C= ENSP00000500264.1:p.Cys252=
ENST00000673284.1:c.756C= ENSP00000499852.1:p.Cys252=
ENST00000345378.6:c.759C= ENSP00000223366.2:p.Cys253=
ENST00000395796.7:c.753C= ENSP00000379142.3:p.Cys251=
ENST00000403799.7:c.756C= ENSP00000384247.3:p.Cys252=
ENST00000437084.1:c.705C= ENSP00000402840.1:p.Cys235=
ENST00000616242.4:c.753C= ENSP00000482149.1:p.Cys251=
NM_000162.3:c.756C= NP_000153.1:p.Cys252=
NM_033507.1:c.759C= NP_277042.1:p.Cys253=
NM_033508.1:c.753C= NP_277043.1:p.Cys251=
XR_927223.1:n.82+9G=
NM_000162.4:c.756C= NP_000153.1:p.Cys252=
NM_001354800.1:c.756C= NP_001341729.1:p.Cys252=
NM_033507.2:c.759C= NP_277042.1:p.Cys253=
NM_033508.2:c.753C= NP_277043.1:p.Cys251=
XR_927223.2:n.82+9G=
NM_000162.5:c.756C= MANE Select NP_000153.1:p.Cys252=
NM_033507.3:c.759C= NP_277042.1:p.Cys253=
NM_033508.3:c.753C= NP_277043.1:p.Cys251=
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