Canonical Allele Identifier: CA1703636000
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150062G= , CM000669.2:g.44150062G= GRCh38
NC_000007.13:g.44189661G= , CM000669.1:g.44189661G= GRCh37
NC_000007.12:g.44156186G= NCBI36
NG_008847.1:g.44362C=
NG_008847.2:g.53109C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*484C= ENSP00000379142.4:n.*484C=
ENST00000616242.5:c.486C= ENSP00000482149.2:p.Gly162=
ENST00000682635.1:n.972C=
ENST00000345378.7:c.489C= ENSP00000223366.2:p.Gly163=
ENST00000403799.8:c.486C= MANE Select ENSP00000384247.3:p.Gly162=
ENST00000671824.1:c.486C= ENSP00000500264.1:p.Gly162=
ENST00000673284.1:c.486C= ENSP00000499852.1:p.Gly162=
ENST00000345378.6:c.489C= ENSP00000223366.2:p.Gly163=
ENST00000395796.7:c.483C= ENSP00000379142.3:p.Gly161=
ENST00000403799.7:c.486C= ENSP00000384247.3:p.Gly162=
ENST00000437084.1:c.435C= ENSP00000402840.1:p.Gly145=
ENST00000616242.4:c.483C= ENSP00000482149.1:p.Gly161=
NM_000162.3:c.486C= NP_000153.1:p.Gly162=
NM_033507.1:c.489C= NP_277042.1:p.Gly163=
NM_033508.1:c.483C= NP_277043.1:p.Gly161=
NM_000162.4:c.486C= NP_000153.1:p.Gly162=
NM_001354800.1:c.486C= NP_001341729.1:p.Gly162=
NM_033507.2:c.489C= NP_277042.1:p.Gly163=
NM_033508.2:c.483C= NP_277043.1:p.Gly161=
NM_000162.5:c.486C= MANE Select NP_000153.1:p.Gly162=
NM_033507.3:c.489C= NP_277042.1:p.Gly163=
NM_033508.3:c.483C= NP_277043.1:p.Gly161=
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