Canonical Allele Identifier: CA1703637571
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153417T= , CM000669.2:g.44153417T= GRCh38
NC_000007.13:g.44193016T= , CM000669.1:g.44193016T= GRCh37
NC_000007.12:g.44159541T= NCBI36
NG_008847.1:g.41007A=
NG_008847.2:g.49754A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*90A= ENSP00000379142.4:n.*90A=
ENST00000616242.5:c.92A= ENSP00000482149.2:p.Lys31=
ENST00000682635.1:n.578A=
ENST00000345378.7:c.95A= ENSP00000223366.2:p.Lys32=
ENST00000403799.8:c.92A= MANE Select ENSP00000384247.3:p.Lys31=
ENST00000671824.1:c.92A= ENSP00000500264.1:p.Lys31=
ENST00000673284.1:c.92A= ENSP00000499852.1:p.Lys31=
ENST00000345378.6:c.95A= ENSP00000223366.2:p.Lys32=
ENST00000395796.7:c.89A= ENSP00000379142.3:p.Lys30=
ENST00000403799.7:c.92A= ENSP00000384247.3:p.Lys31=
ENST00000437084.1:c.92A= ENSP00000402840.1:p.Lys31=
ENST00000476008.1:n.527A=
ENST00000616242.4:c.89A= ENSP00000482149.1:p.Lys30=
NM_000162.3:c.92A= NP_000153.1:p.Lys31=
NM_033507.1:c.95A= NP_277042.1:p.Lys32=
NM_033508.1:c.89A= NP_277043.1:p.Lys30=
NM_000162.4:c.92A= NP_000153.1:p.Lys31=
NM_001354800.1:c.92A= NP_001341729.1:p.Lys31=
NM_033507.2:c.95A= NP_277042.1:p.Lys32=
NM_033508.2:c.89A= NP_277043.1:p.Lys30=
NM_000162.5:c.92A= MANE Select NP_000153.1:p.Lys31=
NM_033507.3:c.95A= NP_277042.1:p.Lys32=
NM_033508.3:c.89A= NP_277043.1:p.Lys30=
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