Canonical Allele Identifier: CA367401725
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 1338246
ClinVar RCV Id: RCV001822844
dbSNP Id: rs2128821636
MyVariant Identifiers: chr7:g.44189636A>C (hg19) chr7:g.44150037A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150037A>C , CM000669.2:g.44150037A>C GRCh38
NC_000007.13:g.44189636A>C , CM000669.1:g.44189636A>C GRCh37
NC_000007.12:g.44156161A>C NCBI36
NG_008847.1:g.44387T>G
NG_008847.2:g.53134T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*509T>G ENSP00000379142.4:n.*509T>G
ENST00000616242.5:c.511T>G ENSP00000482149.2:p.Phe171Val
ENST00000682635.1:n.997T>G
ENST00000345378.7:c.514T>G ENSP00000223366.2:p.Phe172Val
ENST00000403799.8:c.511T>G MANE Select ENSP00000384247.3:p.Phe171Val
ENST00000671824.1:c.511T>G ENSP00000500264.1:p.Phe171Val
ENST00000673284.1:c.511T>G ENSP00000499852.1:p.Phe171Val
ENST00000345378.6:c.514T>G ENSP00000223366.2:p.Phe172Val
ENST00000395796.7:c.508T>G ENSP00000379142.3:p.Phe170Val
ENST00000403799.7:c.511T>G ENSP00000384247.3:p.Phe171Val
ENST00000437084.1:c.460T>G ENSP00000402840.1:p.Phe154Val
ENST00000616242.4:c.508T>G ENSP00000482149.1:p.Phe170Val
NM_000162.3:c.511T>G NP_000153.1:p.Phe171Val
NM_033507.1:c.514T>G NP_277042.1:p.Phe172Val
NM_033508.1:c.508T>G NP_277043.1:p.Phe170Val
NM_000162.4:c.511T>G NP_000153.1:p.Phe171Val
NM_001354800.1:c.511T>G NP_001341729.1:p.Phe171Val
NM_033507.2:c.514T>G NP_277042.1:p.Phe172Val
NM_033508.2:c.508T>G NP_277043.1:p.Phe170Val
NM_000162.5:c.511T>G MANE Select NP_000153.1:p.Phe171Val
NM_033507.3:c.514T>G NP_277042.1:p.Phe172Val
NM_033508.3:c.508T>G NP_277043.1:p.Phe170Val
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