Canonical Allele Identifier: CA1703634878
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147673G= , CM000669.2:g.44147673G= GRCh38
NC_000007.13:g.44187272G= , CM000669.1:g.44187272G= GRCh37
NC_000007.12:g.44153797G= NCBI36
NG_008847.1:g.46751C=
NG_008847.2:g.55498C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*838C= ENSP00000379142.4:n.*838C=
ENST00000616242.5:c.840C= ENSP00000482149.2:p.Ser280=
ENST00000345378.7:c.843C= ENSP00000223366.2:p.Ser281=
ENST00000403799.8:c.840C= MANE Select ENSP00000384247.3:p.Ser280=
ENST00000671824.1:c.840C= ENSP00000500264.1:p.Ser280=
ENST00000673284.1:c.840C= ENSP00000499852.1:p.Ser280=
ENST00000345378.6:c.843C= ENSP00000223366.2:p.Ser281=
ENST00000395796.7:c.837C= ENSP00000379142.3:p.Ser279=
ENST00000403799.7:c.840C= ENSP00000384247.3:p.Ser280=
ENST00000437084.1:c.789C= ENSP00000402840.1:p.Ser263=
ENST00000616242.4:c.837C= ENSP00000482149.1:p.Ser279=
NM_000162.3:c.840C= NP_000153.1:p.Ser280=
NM_033507.1:c.843C= NP_277042.1:p.Ser281=
NM_033508.1:c.837C= NP_277043.1:p.Ser279=
XR_927223.1:n.7G=
NM_000162.4:c.840C= NP_000153.1:p.Ser280=
NM_001354800.1:c.840C= NP_001341729.1:p.Ser280=
NM_033507.2:c.843C= NP_277042.1:p.Ser281=
NM_033508.2:c.837C= NP_277043.1:p.Ser279=
XR_927223.2:n.7G=
NM_000162.5:c.840C= MANE Select NP_000153.1:p.Ser280=
NM_033507.3:c.843C= NP_277042.1:p.Ser281=
NM_033508.3:c.837C= NP_277043.1:p.Ser279=
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