Canonical Allele Identifier: CA213753
Gene: GCK HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 36196
ClinVar RCV Id: RCV000029859
dbSNP Id: rs193922279

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153378C>T , CM000669.2:g.44153378C>T GRCh38
NC_000007.13:g.44192977C>T , CM000669.1:g.44192977C>T GRCh37
NC_000007.12:g.44159502C>T NCBI36
NG_008847.1:g.41046G>A
NG_008847.2:g.49793G>A

Transcript Alleles

HGVS Amino-acid change
NM_000162.3:c.131G>A VV NP_000153.1:p.Gly44Asp
NM_033507.1:c.134G>A VV NP_277042.1:p.Gly45Asp
NM_033508.1:c.128G>A VV NP_277043.1:p.Gly43Asp
NM_000162.4:c.131G>A VV
NM_001354800.1:c.131G>A VV NP_001341729.1:p.Gly44Asp
NM_033507.2:c.134G>A VV
NM_033508.2:c.128G>A VV
NM_000162.5:c.131G>A VV MANE Preferred
ENST00000345378.6:c.134G>A ENSP00000223366.2:p.Gly45Asp
ENST00000395796.7:c.128G>A ENSP00000379142.3:p.Gly43Asp
ENST00000403799.7:c.131G>A ENSP00000384247.3:p.Gly44Asp
ENST00000437084.1:c.131G>A ENSP00000402840.1:p.Gly44Asp
ENST00000616242.4:n.128G>A ENSP00000482149.1:p.Gly43Asp