Canonical Allele Identifier: CA1703612964
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145711G= , CM000669.2:g.44145711G= GRCh38
NC_000007.13:g.44185310G= , CM000669.1:g.44185310G= GRCh37
NC_000007.12:g.44151835G= NCBI36
NG_008847.1:g.48713C=
NG_008847.2:g.57460C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1037C= ENSP00000379142.4:n.*1037C=
ENST00000616242.5:c.*159C= ENSP00000482149.2:n.*159C=
ENST00000683378.1:n.265C=
ENST00000336642.9:c.73C= ENSP00000338009.5:p.Gln25=
ENST00000345378.7:c.1042C= ENSP00000223366.2:p.Gln348=
ENST00000403799.8:c.1039C= MANE Select ENSP00000384247.3:p.Gln347=
ENST00000671824.1:c.1102C= ENSP00000500264.1:p.Gln368=
ENST00000672743.1:n.51C=
ENST00000673284.1:c.1039C= ENSP00000499852.1:p.Gln347=
ENST00000336642.8:c.91C= ENSP00000338009.4:p.Gln31=
ENST00000345378.6:c.1042C= ENSP00000223366.2:p.Gln348=
ENST00000395796.7:c.1036C= ENSP00000379142.3:p.Gln346=
ENST00000403799.7:c.1039C= ENSP00000384247.3:p.Gln347=
ENST00000437084.1:c.988C= ENSP00000402840.1:p.Gln330=
ENST00000459642.1:n.419C=
ENST00000473353.1:n.337C=
ENST00000616242.4:c.1036C= ENSP00000482149.1:p.Gln346=
NM_000162.3:c.1039C= NP_000153.1:p.Gln347=
NM_033507.1:c.1042C= NP_277042.1:p.Gln348=
NM_033508.1:c.1036C= NP_277043.1:p.Gln346=
NM_000162.4:c.1039C= NP_000153.1:p.Gln347=
NM_001354800.1:c.1039C= NP_001341729.1:p.Gln347=
NM_001354801.1:c.28C= NP_001341730.1:p.Gln10=
NM_001354802.1:c.-102C= NP_001341731.1:n.-102C=
NM_001354803.1:c.73C= NP_001341732.1:p.Gln25=
NM_033507.2:c.1042C= NP_277042.1:p.Gln348=
NM_033508.2:c.1036C= NP_277043.1:p.Gln346=
XM_024446707.1:c.-102C= XP_024302475.1:n.-102C=
NM_000162.5:c.1039C= MANE Select NP_000153.1:p.Gln347=
NM_033507.3:c.1042C= NP_277042.1:p.Gln348=
NM_033508.3:c.1036C= NP_277043.1:p.Gln346=
NM_001354803.2:c.73C= NP_001341732.1:p.Gln25=