Canonical Allele Identifier: CA367401962
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44190595A>C (hg19) chr7:g.44150996A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150996A>C , CM000669.2:g.44150996A>C GRCh38
NC_000007.13:g.44190595A>C , CM000669.1:g.44190595A>C GRCh37
NC_000007.12:g.44157120A>C NCBI36
NG_008847.1:g.43428T>G
NG_008847.2:g.52175T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*441T>G ENSP00000379142.4:n.*441T>G
ENST00000616242.5:c.443T>G ENSP00000482149.2:p.Phe148Cys
ENST00000682635.1:n.929T>G
ENST00000345378.7:c.446T>G ENSP00000223366.2:p.Phe149Cys
ENST00000403799.8:c.443T>G MANE Select ENSP00000384247.3:p.Phe148Cys
ENST00000671824.1:c.443T>G ENSP00000500264.1:p.Phe148Cys
ENST00000673284.1:c.443T>G ENSP00000499852.1:p.Phe148Cys
ENST00000345378.6:c.446T>G ENSP00000223366.2:p.Phe149Cys
ENST00000395796.7:c.440T>G ENSP00000379142.3:p.Phe147Cys
ENST00000403799.7:c.443T>G ENSP00000384247.3:p.Phe148Cys
ENST00000437084.1:c.392T>G ENSP00000402840.1:p.Phe131Cys
ENST00000616242.4:c.440T>G ENSP00000482149.1:p.Phe147Cys
NM_000162.3:c.443T>G NP_000153.1:p.Phe148Cys
NM_033507.1:c.446T>G NP_277042.1:p.Phe149Cys
NM_033508.1:c.440T>G NP_277043.1:p.Phe147Cys
NM_000162.4:c.443T>G NP_000153.1:p.Phe148Cys
NM_001354800.1:c.443T>G NP_001341729.1:p.Phe148Cys
NM_033507.2:c.446T>G NP_277042.1:p.Phe149Cys
NM_033508.2:c.440T>G NP_277043.1:p.Phe147Cys
NM_000162.5:c.443T>G MANE Select NP_000153.1:p.Phe148Cys
NM_033507.3:c.446T>G NP_277042.1:p.Phe149Cys
NM_033508.3:c.440T>G NP_277043.1:p.Phe147Cys
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