Canonical Allele Identifier: CA1703612949
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145670C= , CM000669.2:g.44145670C= GRCh38
NC_000007.13:g.44185269C= , CM000669.1:g.44185269C= GRCh37
NC_000007.12:g.44151794C= NCBI36
NG_008847.1:g.48754G=
NG_008847.2:g.57501G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1078G= ENSP00000379142.4:n.*1078G=
ENST00000616242.5:c.*200G= ENSP00000482149.2:n.*200G=
ENST00000683378.1:n.306G=
ENST00000336642.9:c.114G= ENSP00000338009.5:p.Ser38=
ENST00000345378.7:c.1083G= ENSP00000223366.2:p.Ser361=
ENST00000403799.8:c.1080G= MANE Select ENSP00000384247.3:p.Ser360=
ENST00000671824.1:c.1143G= ENSP00000500264.1:p.Ser381=
ENST00000672743.1:n.92G=
ENST00000673284.1:c.1080G= ENSP00000499852.1:p.Ser360=
ENST00000336642.8:c.132G= ENSP00000338009.4:p.Ser44=
ENST00000345378.6:c.1083G= ENSP00000223366.2:p.Ser361=
ENST00000395796.7:c.1077G= ENSP00000379142.3:p.Ser359=
ENST00000403799.7:c.1080G= ENSP00000384247.3:p.Ser360=
ENST00000437084.1:c.1029G= ENSP00000402840.1:p.Ser343=
ENST00000459642.1:n.460G=
ENST00000473353.1:n.378G=
ENST00000616242.4:c.1077G= ENSP00000482149.1:p.Ser359=
NM_000162.3:c.1080G= NP_000153.1:p.Ser360=
NM_033507.1:c.1083G= NP_277042.1:p.Ser361=
NM_033508.1:c.1077G= NP_277043.1:p.Ser359=
NM_000162.4:c.1080G= NP_000153.1:p.Ser360=
NM_001354800.1:c.1080G= NP_001341729.1:p.Ser360=
NM_001354801.1:c.69G= NP_001341730.1:p.Ser23=
NM_001354802.1:c.-61G= NP_001341731.1:n.-61G=
NM_001354803.1:c.114G= NP_001341732.1:p.Ser38=
NM_033507.2:c.1083G= NP_277042.1:p.Ser361=
NM_033508.2:c.1077G= NP_277043.1:p.Ser359=
XM_024446707.1:c.-61G= XP_024302475.1:n.-61G=
NM_000162.5:c.1080G= MANE Select NP_000153.1:p.Ser360=
NM_033507.3:c.1083G= NP_277042.1:p.Ser361=
NM_033508.3:c.1077G= NP_277043.1:p.Ser359=
NM_001354803.2:c.114G= NP_001341732.1:p.Ser38=