Canonical Allele Identifier: CA367401938
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2136526
ClinVar RCV Id: RCV003037221
gnomAD v4: 7-44150988-A-G
MyVariant Identifiers: chr7:g.44190587A>G (hg19) chr7:g.44150988A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150988A>G , CM000669.2:g.44150988A>G GRCh38
NC_000007.13:g.44190587A>G , CM000669.1:g.44190587A>G GRCh37
NC_000007.12:g.44157112A>G NCBI36
NG_008847.1:g.43436T>C
NG_008847.2:g.52183T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*449T>C ENSP00000379142.4:n.*449T>C
ENST00000616242.5:c.451T>C ENSP00000482149.2:p.Ser151Pro
ENST00000682635.1:n.937T>C
ENST00000345378.7:c.454T>C ENSP00000223366.2:p.Ser152Pro
ENST00000403799.8:c.451T>C MANE Select ENSP00000384247.3:p.Ser151Pro
ENST00000671824.1:c.451T>C ENSP00000500264.1:p.Ser151Pro
ENST00000673284.1:c.451T>C ENSP00000499852.1:p.Ser151Pro
ENST00000345378.6:c.454T>C ENSP00000223366.2:p.Ser152Pro
ENST00000395796.7:c.448T>C ENSP00000379142.3:p.Ser150Pro
ENST00000403799.7:c.451T>C ENSP00000384247.3:p.Ser151Pro
ENST00000437084.1:c.400T>C ENSP00000402840.1:p.Ser134Pro
ENST00000616242.4:c.448T>C ENSP00000482149.1:p.Ser150Pro
NM_000162.3:c.451T>C NP_000153.1:p.Ser151Pro
NM_033507.1:c.454T>C NP_277042.1:p.Ser152Pro
NM_033508.1:c.448T>C NP_277043.1:p.Ser150Pro
NM_000162.4:c.451T>C NP_000153.1:p.Ser151Pro
NM_001354800.1:c.451T>C NP_001341729.1:p.Ser151Pro
NM_033507.2:c.454T>C NP_277042.1:p.Ser152Pro
NM_033508.2:c.448T>C NP_277043.1:p.Ser150Pro
NM_000162.5:c.451T>C MANE Select NP_000153.1:p.Ser151Pro
NM_033507.3:c.454T>C NP_277042.1:p.Ser152Pro
NM_033508.3:c.448T>C NP_277043.1:p.Ser150Pro
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