Canonical Allele Identifier: CA1703612939
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145645G= , CM000669.2:g.44145645G= GRCh38
NC_000007.13:g.44185244G= , CM000669.1:g.44185244G= GRCh37
NC_000007.12:g.44151769G= NCBI36
NG_008847.1:g.48779C=
NG_008847.2:g.57526C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1103C= ENSP00000379142.4:n.*1103C=
ENST00000616242.5:c.*225C= ENSP00000482149.2:n.*225C=
ENST00000683378.1:n.331C=
ENST00000336642.9:c.139C= ENSP00000338009.5:p.Arg47=
ENST00000345378.7:c.1108C= ENSP00000223366.2:p.Arg370=
ENST00000403799.8:c.1105C= MANE Select ENSP00000384247.3:p.Arg369=
ENST00000671824.1:c.1168C= ENSP00000500264.1:p.Arg390=
ENST00000672743.1:n.117C=
ENST00000673284.1:c.1105C= ENSP00000499852.1:p.Arg369=
ENST00000336642.8:c.157C= ENSP00000338009.4:p.Arg53=
ENST00000345378.6:c.1108C= ENSP00000223366.2:p.Arg370=
ENST00000395796.7:c.1102C= ENSP00000379142.3:p.Arg368=
ENST00000403799.7:c.1105C= ENSP00000384247.3:p.Arg369=
ENST00000437084.1:c.1054C= ENSP00000402840.1:p.Arg352=
ENST00000459642.1:n.485C=
ENST00000473353.1:n.403C=
ENST00000616242.4:c.1102C= ENSP00000482149.1:p.Arg368=
NM_000162.3:c.1105C= NP_000153.1:p.Arg369=
NM_033507.1:c.1108C= NP_277042.1:p.Arg370=
NM_033508.1:c.1102C= NP_277043.1:p.Arg368=
NM_000162.4:c.1105C= NP_000153.1:p.Arg369=
NM_001354800.1:c.1105C= NP_001341729.1:p.Arg369=
NM_001354801.1:c.94C= NP_001341730.1:p.Arg32=
NM_001354802.1:c.-36C= NP_001341731.1:n.-36C=
NM_001354803.1:c.139C= NP_001341732.1:p.Arg47=
NM_033507.2:c.1108C= NP_277042.1:p.Arg370=
NM_033508.2:c.1102C= NP_277043.1:p.Arg368=
XM_024446707.1:c.-36C= XP_024302475.1:n.-36C=
NM_000162.5:c.1105C= MANE Select NP_000153.1:p.Arg369=
NM_033507.3:c.1108C= NP_277042.1:p.Arg370=
NM_033508.3:c.1102C= NP_277043.1:p.Arg368=
NM_001354803.2:c.139C= NP_001341732.1:p.Arg47=