Canonical Allele Identifier: CA367400461
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2735003
ClinVar RCV Id: RCV003555334
gnomAD v4: 7-44147679-G-T
MyVariant Identifiers: chr7:g.44187278G>T (hg19) chr7:g.44147679G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147679G>T , CM000669.2:g.44147679G>T GRCh38
NC_000007.13:g.44187278G>T , CM000669.1:g.44187278G>T GRCh37
NC_000007.12:g.44153803G>T NCBI36
NG_008847.1:g.46745C>A
NG_008847.2:g.55492C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*832C>A ENSP00000379142.4:n.*832C>A
ENST00000616242.5:c.834C>A ENSP00000482149.2:p.Asp278Glu
ENST00000345378.7:c.837C>A ENSP00000223366.2:p.Asp279Glu
ENST00000403799.8:c.834C>A MANE Select ENSP00000384247.3:p.Asp278Glu
ENST00000671824.1:c.834C>A ENSP00000500264.1:p.Asp278Glu
ENST00000673284.1:c.834C>A ENSP00000499852.1:p.Asp278Glu
ENST00000345378.6:c.837C>A ENSP00000223366.2:p.Asp279Glu
ENST00000395796.7:c.831C>A ENSP00000379142.3:p.Asp277Glu
ENST00000403799.7:c.834C>A ENSP00000384247.3:p.Asp278Glu
ENST00000437084.1:c.783C>A ENSP00000402840.1:p.Asp261Glu
ENST00000616242.4:c.831C>A ENSP00000482149.1:p.Asp277Glu
NM_000162.3:c.834C>A NP_000153.1:p.Asp278Glu
NM_033507.1:c.837C>A NP_277042.1:p.Asp279Glu
NM_033508.1:c.831C>A NP_277043.1:p.Asp277Glu
XR_927223.1:n.13G>T
NM_000162.4:c.834C>A NP_000153.1:p.Asp278Glu
NM_001354800.1:c.834C>A NP_001341729.1:p.Asp278Glu
NM_033507.2:c.837C>A NP_277042.1:p.Asp279Glu
NM_033508.2:c.831C>A NP_277043.1:p.Asp277Glu
XR_927223.2:n.13G>T
NM_000162.5:c.834C>A MANE Select NP_000153.1:p.Asp278Glu
NM_033507.3:c.837C>A NP_277042.1:p.Asp279Glu
NM_033508.3:c.831C>A NP_277043.1:p.Asp277Glu
Search 100 bp 5'
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