Canonical Allele Identifier: CA1100761851
Gene: GCK HGNC NCBI

Linked Data

gnomAD v3: 7-44153501-A-G
gnomAD v4: 7-44153501-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153501A>G , CM000669.2:g.44153501A>G GRCh38
NC_000007.13:g.44193100A>G , CM000669.1:g.44193100A>G GRCh37
NC_000007.12:g.44159625A>G NCBI36
NG_008847.1:g.40923T>C
NG_008847.2:g.49670T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*44-38T>C ENSP00000379142.4:n.*44-38T>C
ENST00000616242.5:c.46-38T>C ENSP00000482149.2:n.46-38T>C
ENST00000682635.1:n.532-38T>C
ENST00000345378.7:c.49-38T>C ENSP00000223366.2:n.49-38T>C
ENST00000403799.8:c.46-38T>C MANE Select ENSP00000384247.3:n.46-38T>C
ENST00000671824.1:c.46-38T>C ENSP00000500264.1:n.46-38T>C
ENST00000673284.1:c.46-38T>C ENSP00000499852.1:n.46-38T>C
ENST00000345378.6:c.49-38T>C ENSP00000223366.2:n.49-38T>C
ENST00000395796.7:c.43-38T>C ENSP00000379142.3:n.43-38T>C
ENST00000403799.7:c.46-38T>C ENSP00000384247.3:n.46-38T>C
ENST00000437084.1:c.46-38T>C ENSP00000402840.1:n.46-38T>C
ENST00000476008.1:n.481-38T>C
ENST00000616242.4:c.43-38T>C ENSP00000482149.1:n.43-38T>C
NM_000162.3:c.46-38T>C NP_000153.1:n.46-38T>C
NM_033507.1:c.49-38T>C NP_277042.1:n.49-38T>C
NM_033508.1:c.43-38T>C NP_277043.1:n.43-38T>C
NM_000162.4:c.46-38T>C NP_000153.1:n.46-38T>C
NM_001354800.1:c.46-38T>C NP_001341729.1:n.46-38T>C
NM_033507.2:c.49-38T>C NP_277042.1:n.49-38T>C
NM_033508.2:c.43-38T>C NP_277043.1:n.43-38T>C
NM_000162.5:c.46-38T>C MANE Select NP_000153.1:n.46-38T>C
NM_033507.3:c.49-38T>C NP_277042.1:n.49-38T>C
NM_033508.3:c.43-38T>C NP_277043.1:n.43-38T>C
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