Canonical Allele Identifier: CA213852
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36257
dbSNP Id: rs193922330

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147734A>G , CM000669.2:g.44147734A>G GRCh38
NC_000007.13:g.44187333A>G , CM000669.1:g.44187333A>G GRCh37
NC_000007.12:g.44153858A>G NCBI36
NG_008847.1:g.46690T>C
NG_008847.2:g.55437T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*777T>C ENSP00000379142.4:n.*777T>C
ENST00000616242.5:c.779T>C ENSP00000482149.2:p.Phe260Ser
ENST00000345378.7:c.782T>C ENSP00000223366.2:p.Phe261Ser
ENST00000403799.8:c.779T>C MANE Select ENSP00000384247.3:p.Phe260Ser
ENST00000671824.1:c.779T>C ENSP00000500264.1:p.Phe260Ser
ENST00000673284.1:c.779T>C ENSP00000499852.1:p.Phe260Ser
ENST00000345378.6:c.782T>C ENSP00000223366.2:p.Phe261Ser
ENST00000395796.7:c.776T>C ENSP00000379142.3:p.Phe259Ser
ENST00000403799.7:c.779T>C ENSP00000384247.3:p.Phe260Ser
ENST00000437084.1:c.728T>C ENSP00000402840.1:p.Phe243Ser
ENST00000616242.4:c.776T>C ENSP00000482149.1:p.Phe259Ser
NM_000162.3:c.779T>C NP_000153.1:p.Phe260Ser
NM_033507.1:c.782T>C NP_277042.1:p.Phe261Ser
NM_033508.1:c.776T>C NP_277043.1:p.Phe259Ser
XR_927223.1:n.68A>G
NM_000162.4:c.779T>C NP_000153.1:p.Phe260Ser
NM_001354800.1:c.779T>C NP_001341729.1:p.Phe260Ser
NM_033507.2:c.782T>C NP_277042.1:p.Phe261Ser
NM_033508.2:c.776T>C NP_277043.1:p.Phe259Ser
XR_927223.2:n.68A>G
NM_000162.5:c.779T>C MANE Select NP_000153.1:p.Phe260Ser
NM_033507.3:c.782T>C NP_277042.1:p.Phe261Ser
NM_033508.3:c.776T>C NP_277043.1:p.Phe259Ser