Canonical Allele Identifier: CA367400526
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44187309T>A (hg19) chr7:g.44147710T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147710T>A , CM000669.2:g.44147710T>A GRCh38
NC_000007.13:g.44187309T>A , CM000669.1:g.44187309T>A GRCh37
NC_000007.12:g.44153834T>A NCBI36
NG_008847.1:g.46714A>T
NG_008847.2:g.55461A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*801A>T ENSP00000379142.4:n.*801A>T
ENST00000616242.5:c.803A>T ENSP00000482149.2:p.Glu268Val
ENST00000345378.7:c.806A>T ENSP00000223366.2:p.Glu269Val
ENST00000403799.8:c.803A>T MANE Select ENSP00000384247.3:p.Glu268Val
ENST00000671824.1:c.803A>T ENSP00000500264.1:p.Glu268Val
ENST00000673284.1:c.803A>T ENSP00000499852.1:p.Glu268Val
ENST00000345378.6:c.806A>T ENSP00000223366.2:p.Glu269Val
ENST00000395796.7:c.800A>T ENSP00000379142.3:p.Glu267Val
ENST00000403799.7:c.803A>T ENSP00000384247.3:p.Glu268Val
ENST00000437084.1:c.752A>T ENSP00000402840.1:p.Glu251Val
ENST00000616242.4:c.800A>T ENSP00000482149.1:p.Glu267Val
NM_000162.3:c.803A>T NP_000153.1:p.Glu268Val
NM_033507.1:c.806A>T NP_277042.1:p.Glu269Val
NM_033508.1:c.800A>T NP_277043.1:p.Glu267Val
XR_927223.1:n.44T>A
NM_000162.4:c.803A>T NP_000153.1:p.Glu268Val
NM_001354800.1:c.803A>T NP_001341729.1:p.Glu268Val
NM_033507.2:c.806A>T NP_277042.1:p.Glu269Val
NM_033508.2:c.800A>T NP_277043.1:p.Glu267Val
XR_927223.2:n.44T>A
NM_000162.5:c.803A>T MANE Select NP_000153.1:p.Glu268Val
NM_033507.3:c.806A>T NP_277042.1:p.Glu269Val
NM_033508.3:c.800A>T NP_277043.1:p.Glu267Val
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