Canonical Allele Identifier: CA367399142
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs1562712960

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145677C>T , CM000669.2:g.44145677C>T GRCh38
NC_000007.13:g.44185276C>T , CM000669.1:g.44185276C>T GRCh37
NC_000007.12:g.44151801C>T NCBI36
NG_008847.1:g.48747G>A
NG_008847.2:g.57494G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1071G>A ENSP00000379142.4:n.*1071G>A
ENST00000616242.5:c.*193G>A ENSP00000482149.2:n.*193G>A
ENST00000683378.1:n.299G>A
ENST00000336642.9:c.107G>A ENSP00000338009.5:p.Arg36Gln
ENST00000345378.7:c.1076G>A ENSP00000223366.2:p.Arg359Gln
ENST00000403799.8:c.1073G>A MANE Select ENSP00000384247.3:p.Arg358Gln
ENST00000671824.1:c.1136G>A ENSP00000500264.1:p.Arg379Gln
ENST00000672743.1:n.85G>A
ENST00000673284.1:c.1073G>A ENSP00000499852.1:p.Arg358Gln
ENST00000336642.8:c.125G>A ENSP00000338009.4:p.Arg42Gln
ENST00000345378.6:c.1076G>A ENSP00000223366.2:p.Arg359Gln
ENST00000395796.7:c.1070G>A ENSP00000379142.3:p.Arg357Gln
ENST00000403799.7:c.1073G>A ENSP00000384247.3:p.Arg358Gln
ENST00000437084.1:c.1022G>A ENSP00000402840.1:p.Arg341Gln
ENST00000459642.1:n.453G>A
ENST00000473353.1:n.371G>A
ENST00000616242.4:c.1070G>A ENSP00000482149.1:p.Arg357Gln
NM_000162.3:c.1073G>A NP_000153.1:p.Arg358Gln
NM_033507.1:c.1076G>A NP_277042.1:p.Arg359Gln
NM_033508.1:c.1070G>A NP_277043.1:p.Arg357Gln
NM_000162.4:c.1073G>A NP_000153.1:p.Arg358Gln
NM_001354800.1:c.1073G>A NP_001341729.1:p.Arg358Gln
NM_001354801.1:c.62G>A NP_001341730.1:p.Arg21Gln
NM_001354802.1:c.-68G>A NP_001341731.1:n.-68G>A
NM_001354803.1:c.107G>A NP_001341732.1:p.Arg36Gln
NM_033507.2:c.1076G>A NP_277042.1:p.Arg359Gln
NM_033508.2:c.1070G>A NP_277043.1:p.Arg357Gln
XM_024446707.1:c.-68G>A XP_024302475.1:n.-68G>A
NM_000162.5:c.1073G>A MANE Select NP_000153.1:p.Arg358Gln
NM_033507.3:c.1076G>A NP_277042.1:p.Arg359Gln
NM_033508.3:c.1070G>A NP_277043.1:p.Arg357Gln
NM_001354803.2:c.107G>A NP_001341732.1:p.Arg36Gln