Canonical Allele Identifier: CA10581225
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 235097
ClinVar RCV Id: RCV000223803 RCV003556284
dbSNP Id: rs876661320
MyVariant Identifiers: chr7:g.44193019A>G (hg19) chr7:g.44153420A>G (hg38)
PubMed: PMID:28555465
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153420A>G , CM000669.2:g.44153420A>G GRCh38
NC_000007.13:g.44193019A>G , CM000669.1:g.44193019A>G GRCh37
NC_000007.12:g.44159544A>G NCBI36
NG_008847.1:g.41004T>C
NG_008847.2:g.49751T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*87T>C ENSP00000379142.4:n.*87T>C
ENST00000616242.5:c.89T>C ENSP00000482149.2:p.Leu30Pro
ENST00000682635.1:n.575T>C
ENST00000345378.7:c.92T>C ENSP00000223366.2:p.Leu31Pro
ENST00000403799.8:c.89T>C MANE Select ENSP00000384247.3:p.Leu30Pro
ENST00000671824.1:c.89T>C ENSP00000500264.1:p.Leu30Pro
ENST00000673284.1:c.89T>C ENSP00000499852.1:p.Leu30Pro
ENST00000345378.6:c.92T>C ENSP00000223366.2:p.Leu31Pro
ENST00000395796.7:c.86T>C ENSP00000379142.3:p.Leu29Pro
ENST00000403799.7:c.89T>C ENSP00000384247.3:p.Leu30Pro
ENST00000437084.1:c.89T>C ENSP00000402840.1:p.Leu30Pro
ENST00000476008.1:n.524T>C
ENST00000616242.4:c.86T>C ENSP00000482149.1:p.Leu29Pro
NM_000162.3:c.89T>C NP_000153.1:p.Leu30Pro
NM_033507.1:c.92T>C NP_277042.1:p.Leu31Pro
NM_033508.1:c.86T>C NP_277043.1:p.Leu29Pro
NM_000162.4:c.89T>C NP_000153.1:p.Leu30Pro
NM_001354800.1:c.89T>C NP_001341729.1:p.Leu30Pro
NM_033507.2:c.92T>C NP_277042.1:p.Leu31Pro
NM_033508.2:c.86T>C NP_277043.1:p.Leu29Pro
NM_000162.5:c.89T>C MANE Select NP_000153.1:p.Leu30Pro
NM_033507.3:c.92T>C NP_277042.1:p.Leu31Pro
NM_033508.3:c.86T>C NP_277043.1:p.Leu29Pro
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