Canonical Allele Identifier: CA1703612933
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145636C= , CM000669.2:g.44145636C= GRCh38
NC_000007.13:g.44185235C= , CM000669.1:g.44185235C= GRCh37
NC_000007.12:g.44151760C= NCBI36
NG_008847.1:g.48788G=
NG_008847.2:g.57535G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1112G= ENSP00000379142.4:n.*1112G=
ENST00000616242.5:c.*234G= ENSP00000482149.2:n.*234G=
ENST00000683378.1:n.340G=
ENST00000336642.9:c.148G= ENSP00000338009.5:p.Glu50=
ENST00000345378.7:c.1117G= ENSP00000223366.2:p.Glu373=
ENST00000403799.8:c.1114G= MANE Select ENSP00000384247.3:p.Glu372=
ENST00000671824.1:c.1177G= ENSP00000500264.1:p.Glu393=
ENST00000672743.1:n.126G=
ENST00000673284.1:c.1114G= ENSP00000499852.1:p.Glu372=
ENST00000336642.8:c.166G= ENSP00000338009.4:p.Glu56=
ENST00000345378.6:c.1117G= ENSP00000223366.2:p.Glu373=
ENST00000395796.7:c.1111G= ENSP00000379142.3:p.Glu371=
ENST00000403799.7:c.1114G= ENSP00000384247.3:p.Glu372=
ENST00000437084.1:c.1063G= ENSP00000402840.1:p.Glu355=
ENST00000459642.1:n.494G=
ENST00000616242.4:c.1111G= ENSP00000482149.1:p.Glu371=
NM_000162.3:c.1114G= NP_000153.1:p.Glu372=
NM_033507.1:c.1117G= NP_277042.1:p.Glu373=
NM_033508.1:c.1111G= NP_277043.1:p.Glu371=
NM_000162.4:c.1114G= NP_000153.1:p.Glu372=
NM_001354800.1:c.1114G= NP_001341729.1:p.Glu372=
NM_001354801.1:c.103G= NP_001341730.1:p.Glu35=
NM_001354802.1:c.-27G= NP_001341731.1:n.-27G=
NM_001354803.1:c.148G= NP_001341732.1:p.Glu50=
NM_033507.2:c.1117G= NP_277042.1:p.Glu373=
NM_033508.2:c.1111G= NP_277043.1:p.Glu371=
XM_024446707.1:c.-27G= XP_024302475.1:n.-27G=
NM_000162.5:c.1114G= MANE Select NP_000153.1:p.Glu372=
NM_033507.3:c.1117G= NP_277042.1:p.Glu373=
NM_033508.3:c.1111G= NP_277043.1:p.Glu371=
NM_001354803.2:c.148G= NP_001341732.1:p.Glu50=