Canonical Allele Identifier: CA16618472
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 419624
dbSNP Id: rs1064793998
gnomAD v4: 7-44153325-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153325C>T , CM000669.2:g.44153325C>T GRCh38
NC_000007.13:g.44192924C>T , CM000669.1:g.44192924C>T GRCh37
NC_000007.12:g.44159449C>T NCBI36
NG_008847.1:g.41099G>A
NG_008847.2:g.49846G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*182G>A ENSP00000379142.4:n.*182G>A
ENST00000616242.5:c.184G>A ENSP00000482149.2:p.Val62Met
ENST00000682635.1:n.670G>A
ENST00000345378.7:c.187G>A ENSP00000223366.2:p.Val63Met
ENST00000403799.8:c.184G>A MANE Select ENSP00000384247.3:p.Val62Met
ENST00000671824.1:c.184G>A ENSP00000500264.1:p.Val62Met
ENST00000673284.1:c.184G>A ENSP00000499852.1:p.Val62Met
ENST00000345378.6:c.187G>A ENSP00000223366.2:p.Val63Met
ENST00000395796.7:c.181G>A ENSP00000379142.3:p.Val61Met
ENST00000403799.7:c.184G>A ENSP00000384247.3:p.Val62Met
ENST00000437084.1:c.184G>A ENSP00000402840.1:p.Val62Met
ENST00000616242.4:c.181G>A ENSP00000482149.1:p.Val61Met
NM_000162.3:c.184G>A NP_000153.1:p.Val62Met
NM_033507.1:c.187G>A NP_277042.1:p.Val63Met
NM_033508.1:c.181G>A NP_277043.1:p.Val61Met
NM_000162.4:c.184G>A NP_000153.1:p.Val62Met
NM_001354800.1:c.184G>A NP_001341729.1:p.Val62Met
NM_033507.2:c.187G>A NP_277042.1:p.Val63Met
NM_033508.2:c.181G>A NP_277043.1:p.Val61Met
NM_000162.5:c.184G>A MANE Select NP_000153.1:p.Val62Met
NM_033507.3:c.187G>A NP_277042.1:p.Val63Met
NM_033508.3:c.181G>A NP_277043.1:p.Val61Met