Canonical Allele Identifier: CA1703635967
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149987G= , CM000669.2:g.44149987G= GRCh38
NC_000007.13:g.44189586G= , CM000669.1:g.44189586G= GRCh37
NC_000007.12:g.44156111G= NCBI36
NG_008847.1:g.44437C=
NG_008847.2:g.53184C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*559C= ENSP00000379142.4:n.*559C=
ENST00000616242.5:c.561C= ENSP00000482149.2:p.Asp187=
ENST00000682635.1:n.1047C=
ENST00000345378.7:c.564C= ENSP00000223366.2:p.Asp188=
ENST00000403799.8:c.561C= MANE Select ENSP00000384247.3:p.Asp187=
ENST00000671824.1:c.561C= ENSP00000500264.1:p.Asp187=
ENST00000673284.1:c.561C= ENSP00000499852.1:p.Asp187=
ENST00000345378.6:c.564C= ENSP00000223366.2:p.Asp188=
ENST00000395796.7:c.558C= ENSP00000379142.3:p.Asp186=
ENST00000403799.7:c.561C= ENSP00000384247.3:p.Asp187=
ENST00000437084.1:c.510C= ENSP00000402840.1:p.Asp170=
ENST00000616242.4:c.558C= ENSP00000482149.1:p.Asp186=
NM_000162.3:c.561C= NP_000153.1:p.Asp187=
NM_033507.1:c.564C= NP_277042.1:p.Asp188=
NM_033508.1:c.558C= NP_277043.1:p.Asp186=
NM_000162.4:c.561C= NP_000153.1:p.Asp187=
NM_001354800.1:c.561C= NP_001341729.1:p.Asp187=
NM_033507.2:c.564C= NP_277042.1:p.Asp188=
NM_033508.2:c.558C= NP_277043.1:p.Asp186=
NM_000162.5:c.561C= MANE Select NP_000153.1:p.Asp187=
NM_033507.3:c.564C= NP_277042.1:p.Asp188=
NM_033508.3:c.558C= NP_277043.1:p.Asp186=
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