Canonical Allele Identifier: CA367403782
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs2096283320
gnomAD v4: 7-44153444-T-C
MyVariant Identifiers: chr7:g.44193043T>C (hg19) chr7:g.44153444T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153444T>C , CM000669.2:g.44153444T>C GRCh38
NC_000007.13:g.44193043T>C , CM000669.1:g.44193043T>C GRCh37
NC_000007.12:g.44159568T>C NCBI36
NG_008847.1:g.40980A>G
NG_008847.2:g.49727A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*63A>G ENSP00000379142.4:n.*63A>G
ENST00000616242.5:c.65A>G ENSP00000482149.2:p.Glu22Gly
ENST00000682635.1:n.551A>G
ENST00000345378.7:c.68A>G ENSP00000223366.2:p.Glu23Gly
ENST00000403799.8:c.65A>G MANE Select ENSP00000384247.3:p.Glu22Gly
ENST00000671824.1:c.65A>G ENSP00000500264.1:p.Glu22Gly
ENST00000673284.1:c.65A>G ENSP00000499852.1:p.Glu22Gly
ENST00000345378.6:c.68A>G ENSP00000223366.2:p.Glu23Gly
ENST00000395796.7:c.62A>G ENSP00000379142.3:p.Glu21Gly
ENST00000403799.7:c.65A>G ENSP00000384247.3:p.Glu22Gly
ENST00000437084.1:c.65A>G ENSP00000402840.1:p.Glu22Gly
ENST00000476008.1:n.500A>G
ENST00000616242.4:c.62A>G ENSP00000482149.1:p.Glu21Gly
NM_000162.3:c.65A>G NP_000153.1:p.Glu22Gly
NM_033507.1:c.68A>G NP_277042.1:p.Glu23Gly
NM_033508.1:c.62A>G NP_277043.1:p.Glu21Gly
NM_000162.4:c.65A>G NP_000153.1:p.Glu22Gly
NM_001354800.1:c.65A>G NP_001341729.1:p.Glu22Gly
NM_033507.2:c.68A>G NP_277042.1:p.Glu23Gly
NM_033508.2:c.62A>G NP_277043.1:p.Glu21Gly
NM_000162.5:c.65A>G MANE Select NP_000153.1:p.Glu22Gly
NM_033507.3:c.68A>G NP_277042.1:p.Glu23Gly
NM_033508.3:c.62A>G NP_277043.1:p.Glu21Gly
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