Canonical Allele Identifier: CA1703634766
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147479G= , CM000669.2:g.44147479G= GRCh38
NC_000007.13:g.44187078G= , CM000669.1:g.44187078G= GRCh37
NC_000007.12:g.44153603G= NCBI36
NG_008847.1:g.46945C=
NG_008847.2:g.55692C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*861+171C= ENSP00000379142.4:n.*861+171C=
ENST00000616242.5:c.853+181C= ENSP00000482149.2:n.853+181C=
ENST00000345378.7:c.866+171C= ENSP00000223366.2:n.866+171C=
ENST00000403799.8:c.863+171C= MANE Select ENSP00000384247.3:n.863+171C=
ENST00000671824.1:c.854-66C= ENSP00000500264.1:n.854-66C=
ENST00000673284.1:c.863+171C= ENSP00000499852.1:n.863+171C=
ENST00000345378.6:c.866+171C= ENSP00000223366.2:n.866+171C=
ENST00000395796.7:c.860+171C= ENSP00000379142.3:n.860+171C=
ENST00000403799.7:c.863+171C= ENSP00000384247.3:n.863+171C=
ENST00000437084.1:c.812+171C= ENSP00000402840.1:n.812+171C=
ENST00000616242.4:c.860+171C= ENSP00000482149.1:n.860+171C=
NM_000162.3:c.863+171C= NP_000153.1:n.863+171C=
NM_033507.1:c.866+171C= NP_277042.1:n.866+171C=
NM_033508.1:c.860+171C= NP_277043.1:n.860+171C=
NM_000162.4:c.863+171C= NP_000153.1:n.863+171C=
NM_001354800.1:c.863+171C= NP_001341729.1:n.863+171C=
NM_033507.2:c.866+171C= NP_277042.1:n.866+171C=
NM_033508.2:c.860+171C= NP_277043.1:n.860+171C=
NM_000162.5:c.863+171C= MANE Select NP_000153.1:n.863+171C=
NM_033507.3:c.866+171C= NP_277042.1:n.866+171C=
NM_033508.3:c.860+171C= NP_277043.1:n.860+171C=
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