Canonical Allele Identifier: CA1703612929
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145630C= , CM000669.2:g.44145630C= GRCh38
NC_000007.13:g.44185229C= , CM000669.1:g.44185229C= GRCh37
NC_000007.12:g.44151754C= NCBI36
NG_008847.1:g.48794G=
NG_008847.2:g.57541G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1118G= ENSP00000379142.4:n.*1118G=
ENST00000616242.5:c.*240G= ENSP00000482149.2:n.*240G=
ENST00000683378.1:n.346G=
ENST00000336642.9:c.154G= ENSP00000338009.5:p.Val52=
ENST00000345378.7:c.1123G= ENSP00000223366.2:p.Val375=
ENST00000403799.8:c.1120G= MANE Select ENSP00000384247.3:p.Val374=
ENST00000671824.1:c.1183G= ENSP00000500264.1:p.Val395=
ENST00000672743.1:n.132G=
ENST00000673284.1:c.1120G= ENSP00000499852.1:p.Val374=
ENST00000336642.8:c.172G= ENSP00000338009.4:p.Val58=
ENST00000345378.6:c.1123G= ENSP00000223366.2:p.Val375=
ENST00000395796.7:c.1117G= ENSP00000379142.3:p.Val373=
ENST00000403799.7:c.1120G= ENSP00000384247.3:p.Val374=
ENST00000437084.1:c.1069G= ENSP00000402840.1:p.Val357=
ENST00000459642.1:n.500G=
ENST00000616242.4:c.1117G= ENSP00000482149.1:p.Val373=
NM_000162.3:c.1120G= NP_000153.1:p.Val374=
NM_033507.1:c.1123G= NP_277042.1:p.Val375=
NM_033508.1:c.1117G= NP_277043.1:p.Val373=
NM_000162.4:c.1120G= NP_000153.1:p.Val374=
NM_001354800.1:c.1120G= NP_001341729.1:p.Val374=
NM_001354801.1:c.109G= NP_001341730.1:p.Val37=
NM_001354802.1:c.-21G= NP_001341731.1:n.-21G=
NM_001354803.1:c.154G= NP_001341732.1:p.Val52=
NM_033507.2:c.1123G= NP_277042.1:p.Val375=
NM_033508.2:c.1117G= NP_277043.1:p.Val373=
XM_024446707.1:c.-21G= XP_024302475.1:n.-21G=
NM_000162.5:c.1120G= MANE Select NP_000153.1:p.Val374=
NM_033507.3:c.1123G= NP_277042.1:p.Val375=
NM_033508.3:c.1117G= NP_277043.1:p.Val373=
NM_001354803.2:c.154G= NP_001341732.1:p.Val52=