Canonical Allele Identifier: CA367400140
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 447423
dbSNP Id: rs1554334905

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44146599C>T , CM000669.2:g.44146599C>T GRCh38
NC_000007.13:g.44186198C>T , CM000669.1:g.44186198C>T GRCh37
NC_000007.12:g.44152723C>T NCBI36
NG_008847.1:g.47825G>A
NG_008847.2:g.56572G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*881G>A ENSP00000379142.4:n.*881G>A
ENST00000616242.5:c.*3G>A ENSP00000482149.2:n.*3G>A
ENST00000683378.1:n.109G>A
ENST00000345378.7:c.886G>A ENSP00000223366.2:p.Gly296Ser
ENST00000403799.8:c.883G>A MANE Select ENSP00000384247.3:p.Gly295Ser
ENST00000671824.1:c.946G>A ENSP00000500264.1:p.Gly316Ser
ENST00000673284.1:c.883G>A ENSP00000499852.1:p.Gly295Ser
ENST00000345378.6:c.886G>A ENSP00000223366.2:p.Gly296Ser
ENST00000395796.7:c.880G>A ENSP00000379142.3:p.Gly294Ser
ENST00000403799.7:c.883G>A ENSP00000384247.3:p.Gly295Ser
ENST00000437084.1:c.832G>A ENSP00000402840.1:p.Gly278Ser
ENST00000473353.1:n.181G>A
ENST00000616242.4:c.880G>A ENSP00000482149.1:p.Gly294Ser
NM_000162.3:c.883G>A NP_000153.1:p.Gly295Ser
NM_033507.1:c.886G>A NP_277042.1:p.Gly296Ser
NM_033508.1:c.880G>A NP_277043.1:p.Gly294Ser
NM_000162.4:c.883G>A NP_000153.1:p.Gly295Ser
NM_001354800.1:c.883G>A NP_001341729.1:p.Gly295Ser
NM_001354801.1:c.8+20G>A NP_001341730.1:n.8+20G>A
NM_033507.2:c.886G>A NP_277042.1:p.Gly296Ser
NM_033508.2:c.880G>A NP_277043.1:p.Gly294Ser
NM_000162.5:c.883G>A MANE Select NP_000153.1:p.Gly295Ser
NM_033507.3:c.886G>A NP_277042.1:p.Gly296Ser
NM_033508.3:c.880G>A NP_277043.1:p.Gly294Ser