Canonical Allele Identifier: CA454863119
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs755112715
gnomAD v4: 7-44145517-G-T
MyVariant Identifiers: chr7:g.44185116G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145517G>T , CM000669.2:g.44145517G>T GRCh38
NC_000007.13:g.44185116G>T , CM000669.1:g.44185116G>T GRCh37
NC_000007.12:g.44151641G>T NCBI36
NG_008847.1:g.48907C>A
NG_008847.2:g.57654C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1231C>A ENSP00000379142.4:n.*1231C>A
ENST00000616242.5:c.*353C>A ENSP00000482149.2:n.*353C>A
ENST00000683378.1:n.459C>A
ENST00000336642.9:c.267C>A ENSP00000338009.5:p.Ser89=
ENST00000345378.7:c.1236C>A ENSP00000223366.2:p.Ser412=
ENST00000403799.8:c.1233C>A MANE Select ENSP00000384247.3:p.Ser411=
ENST00000671824.1:c.1296C>A ENSP00000500264.1:p.Ser432=
ENST00000672743.1:n.245C>A
ENST00000673284.1:c.1233C>A ENSP00000499852.1:p.Ser411=
ENST00000336642.8:c.285C>A ENSP00000338009.4:p.Ser95=
ENST00000345378.6:c.1236C>A ENSP00000223366.2:p.Ser412=
ENST00000395796.7:c.1230C>A ENSP00000379142.3:p.Ser410=
ENST00000403799.7:c.1233C>A ENSP00000384247.3:p.Ser411=
ENST00000437084.1:c.1182C>A ENSP00000402840.1:p.Ser394=
ENST00000459642.1:n.613C>A
ENST00000616242.4:c.1230C>A ENSP00000482149.1:p.Ser410=
NM_000162.3:c.1233C>A NP_000153.1:p.Ser411=
NM_033507.1:c.1236C>A NP_277042.1:p.Ser412=
NM_033508.1:c.1230C>A NP_277043.1:p.Ser410=
NM_000162.4:c.1233C>A NP_000153.1:p.Ser411=
NM_001354800.1:c.1233C>A NP_001341729.1:p.Ser411=
NM_001354801.1:c.222C>A NP_001341730.1:p.Ser74=
NM_001354802.1:c.93C>A NP_001341731.1:p.Ser31=
NM_001354803.1:c.267C>A NP_001341732.1:p.Ser89=
NM_033507.2:c.1236C>A NP_277042.1:p.Ser412=
NM_033508.2:c.1230C>A NP_277043.1:p.Ser410=
XM_024446707.1:c.93C>A XP_024302475.1:p.Ser31=
NM_000162.5:c.1233C>A MANE Select NP_000153.1:p.Ser411=
NM_033507.3:c.1236C>A NP_277042.1:p.Ser412=
NM_033508.3:c.1230C>A NP_277043.1:p.Ser410=
NM_001354803.2:c.267C>A NP_001341732.1:p.Ser89=
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