Canonical Allele Identifier: CA367401952
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44190592G>C (hg19) chr7:g.44150993G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150993G>C , CM000669.2:g.44150993G>C GRCh38
NC_000007.13:g.44190592G>C , CM000669.1:g.44190592G>C GRCh37
NC_000007.12:g.44157117G>C NCBI36
NG_008847.1:g.43431C>G
NG_008847.2:g.52178C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*444C>G ENSP00000379142.4:n.*444C>G
ENST00000616242.5:c.446C>G ENSP00000482149.2:p.Thr149Ser
ENST00000682635.1:n.932C>G
ENST00000345378.7:c.449C>G ENSP00000223366.2:p.Thr150Ser
ENST00000403799.8:c.446C>G MANE Select ENSP00000384247.3:p.Thr149Ser
ENST00000671824.1:c.446C>G ENSP00000500264.1:p.Thr149Ser
ENST00000673284.1:c.446C>G ENSP00000499852.1:p.Thr149Ser
ENST00000345378.6:c.449C>G ENSP00000223366.2:p.Thr150Ser
ENST00000395796.7:c.443C>G ENSP00000379142.3:p.Thr148Ser
ENST00000403799.7:c.446C>G ENSP00000384247.3:p.Thr149Ser
ENST00000437084.1:c.395C>G ENSP00000402840.1:p.Thr132Ser
ENST00000616242.4:c.443C>G ENSP00000482149.1:p.Thr148Ser
NM_000162.3:c.446C>G NP_000153.1:p.Thr149Ser
NM_033507.1:c.449C>G NP_277042.1:p.Thr150Ser
NM_033508.1:c.443C>G NP_277043.1:p.Thr148Ser
NM_000162.4:c.446C>G NP_000153.1:p.Thr149Ser
NM_001354800.1:c.446C>G NP_001341729.1:p.Thr149Ser
NM_033507.2:c.449C>G NP_277042.1:p.Thr150Ser
NM_033508.2:c.443C>G NP_277043.1:p.Thr148Ser
NM_000162.5:c.446C>G MANE Select NP_000153.1:p.Thr149Ser
NM_033507.3:c.449C>G NP_277042.1:p.Thr150Ser
NM_033508.3:c.443C>G NP_277043.1:p.Thr148Ser
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