Canonical Allele Identifier: CA454863269
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44185224A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145625A>T , CM000669.2:g.44145625A>T GRCh38
NC_000007.13:g.44185224A>T , CM000669.1:g.44185224A>T GRCh37
NC_000007.12:g.44151749A>T NCBI36
NG_008847.1:g.48799T>A
NG_008847.2:g.57546T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1123T>A ENSP00000379142.4:n.*1123T>A
ENST00000616242.5:c.*245T>A ENSP00000482149.2:n.*245T>A
ENST00000683378.1:n.351T>A
ENST00000336642.9:c.159T>A ENSP00000338009.5:p.Ser53=
ENST00000345378.7:c.1128T>A ENSP00000223366.2:p.Ser376=
ENST00000403799.8:c.1125T>A MANE Select ENSP00000384247.3:p.Ser375=
ENST00000671824.1:c.1188T>A ENSP00000500264.1:p.Ser396=
ENST00000672743.1:n.137T>A
ENST00000673284.1:c.1125T>A ENSP00000499852.1:p.Ser375=
ENST00000336642.8:c.177T>A ENSP00000338009.4:p.Ser59=
ENST00000345378.6:c.1128T>A ENSP00000223366.2:p.Ser376=
ENST00000395796.7:c.1122T>A ENSP00000379142.3:p.Ser374=
ENST00000403799.7:c.1125T>A ENSP00000384247.3:p.Ser375=
ENST00000437084.1:c.1074T>A ENSP00000402840.1:p.Ser358=
ENST00000459642.1:n.505T>A
ENST00000616242.4:c.1122T>A ENSP00000482149.1:p.Ser374=
NM_000162.3:c.1125T>A NP_000153.1:p.Ser375=
NM_033507.1:c.1128T>A NP_277042.1:p.Ser376=
NM_033508.1:c.1122T>A NP_277043.1:p.Ser374=
NM_000162.4:c.1125T>A NP_000153.1:p.Ser375=
NM_001354800.1:c.1125T>A NP_001341729.1:p.Ser375=
NM_001354801.1:c.114T>A NP_001341730.1:p.Ser38=
NM_001354802.1:c.-16T>A NP_001341731.1:n.-16T>A
NM_001354803.1:c.159T>A NP_001341732.1:p.Ser53=
NM_033507.2:c.1128T>A NP_277042.1:p.Ser376=
NM_033508.2:c.1122T>A NP_277043.1:p.Ser374=
XM_024446707.1:c.-16T>A XP_024302475.1:n.-16T>A
NM_000162.5:c.1125T>A MANE Select NP_000153.1:p.Ser375=
NM_033507.3:c.1128T>A NP_277042.1:p.Ser376=
NM_033508.3:c.1122T>A NP_277043.1:p.Ser374=
NM_001354803.2:c.159T>A NP_001341732.1:p.Ser53=
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