Canonical Allele Identifier: CA1703612688
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145231C= , CM000669.2:g.44145231C= GRCh38
NC_000007.13:g.44184830C= , CM000669.1:g.44184830C= GRCh37
NC_000007.12:g.44151355C= NCBI36
NG_008847.1:g.49193G=
NG_008847.2:g.57940G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1301G= ENSP00000379142.4:n.*1301G=
ENST00000616242.5:c.*423G= ENSP00000482149.2:n.*423G=
ENST00000683378.1:n.529G=
ENST00000336642.9:c.337G= ENSP00000338009.5:p.Glu113=
ENST00000345378.7:c.1306G= ENSP00000223366.2:p.Glu436=
ENST00000403799.8:c.1303G= MANE Select ENSP00000384247.3:p.Glu435=
ENST00000671824.1:c.1366G= ENSP00000500264.1:p.Glu456=
ENST00000672743.1:n.315G=
ENST00000673284.1:c.1303G= ENSP00000499852.1:p.Glu435=
ENST00000336642.8:c.355G= ENSP00000338009.4:p.Glu119=
ENST00000345378.6:c.1306G= ENSP00000223366.2:p.Glu436=
ENST00000395796.7:c.1300G= ENSP00000379142.3:p.Glu434=
ENST00000403799.7:c.1303G= ENSP00000384247.3:p.Glu435=
ENST00000437084.1:c.1252G= ENSP00000402840.1:p.Glu418=
ENST00000459642.1:n.683G=
ENST00000616242.4:c.1300G= ENSP00000482149.1:p.Glu434=
NM_000162.3:c.1303G= NP_000153.1:p.Glu435=
NM_033507.1:c.1306G= NP_277042.1:p.Glu436=
NM_033508.1:c.1300G= NP_277043.1:p.Glu434=
NM_000162.4:c.1303G= NP_000153.1:p.Glu435=
NM_001354800.1:c.1303G= NP_001341729.1:p.Glu435=
NM_001354801.1:c.292G= NP_001341730.1:p.Glu98=
NM_001354802.1:c.163G= NP_001341731.1:p.Glu55=
NM_001354803.1:c.337G= NP_001341732.1:p.Glu113=
NM_033507.2:c.1306G= NP_277042.1:p.Glu436=
NM_033508.2:c.1300G= NP_277043.1:p.Glu434=
XM_024446707.1:c.163G= XP_024302475.1:p.Glu55=
NM_000162.5:c.1303G= MANE Select NP_000153.1:p.Glu435=
NM_033507.3:c.1306G= NP_277042.1:p.Glu436=
NM_033508.3:c.1300G= NP_277043.1:p.Glu434=
NM_001354803.2:c.337G= NP_001341732.1:p.Glu113=