Canonical Allele Identifier: CA1703612639
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145143C= , CM000669.2:g.44145143C= GRCh38
NC_000007.13:g.44184742C= , CM000669.1:g.44184742C= GRCh37
NC_000007.12:g.44151267C= NCBI36
NG_008847.1:g.49281G=
NG_008847.2:g.58028G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1389G= ENSP00000379142.4:n.*1389G=
ENST00000616242.5:c.*511G= ENSP00000482149.2:n.*511G=
ENST00000683378.1:n.617G=
ENST00000336642.9:c.425G= ENSP00000338009.5:p.Gly142=
ENST00000345378.7:c.1394G= ENSP00000223366.2:p.Gly465=
ENST00000403799.8:c.1391G= MANE Select ENSP00000384247.3:p.Gly464=
ENST00000671824.1:c.1454G= ENSP00000500264.1:p.Gly485=
ENST00000672743.1:n.381+22G=
ENST00000673284.1:c.1369+22G= ENSP00000499852.1:n.1369+22G=
ENST00000336642.8:c.443G= ENSP00000338009.4:p.Gly148=
ENST00000345378.6:c.1394G= ENSP00000223366.2:p.Gly465=
ENST00000395796.7:c.1388G= ENSP00000379142.3:p.Gly463=
ENST00000403799.7:c.1391G= ENSP00000384247.3:p.Gly464=
ENST00000437084.1:c.1340G= ENSP00000402840.1:p.Gly447=
ENST00000459642.1:n.771G=
ENST00000616242.4:c.1388G= ENSP00000482149.1:p.Gly463=
NM_000162.3:c.1391G= NP_000153.1:p.Gly464=
NM_033507.1:c.1394G= NP_277042.1:p.Gly465=
NM_033508.1:c.1388G= NP_277043.1:p.Gly463=
NM_000162.4:c.1391G= NP_000153.1:p.Gly464=
NM_001354800.1:c.1369+22G= NP_001341729.1:n.1369+22G=
NM_001354801.1:c.380G= NP_001341730.1:p.Gly127=
NM_001354802.1:c.229+22G= NP_001341731.1:n.229+22G=
NM_001354803.1:c.425G= NP_001341732.1:p.Gly142=
NM_033507.2:c.1394G= NP_277042.1:p.Gly465=
NM_033508.2:c.1388G= NP_277043.1:p.Gly463=
XM_024446707.1:c.251G= XP_024302475.1:p.Gly84=
NM_000162.5:c.1391G= MANE Select NP_000153.1:p.Gly464=
NM_033507.3:c.1394G= NP_277042.1:p.Gly465=
NM_033508.3:c.1388G= NP_277043.1:p.Gly463=
NM_001354803.2:c.425G= NP_001341732.1:p.Gly142=