Canonical Allele Identifier: CA1703612931
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145632C= , CM000669.2:g.44145632C= GRCh38
NC_000007.13:g.44185231C= , CM000669.1:g.44185231C= GRCh37
NC_000007.12:g.44151756C= NCBI36
NG_008847.1:g.48792G=
NG_008847.2:g.57539G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1116G= ENSP00000379142.4:n.*1116G=
ENST00000616242.5:c.*238G= ENSP00000482149.2:n.*238G=
ENST00000683378.1:n.344G=
ENST00000336642.9:c.152G= ENSP00000338009.5:p.Ser51=
ENST00000345378.7:c.1121G= ENSP00000223366.2:p.Ser374=
ENST00000403799.8:c.1118G= MANE Select ENSP00000384247.3:p.Ser373=
ENST00000671824.1:c.1181G= ENSP00000500264.1:p.Ser394=
ENST00000672743.1:n.130G=
ENST00000673284.1:c.1118G= ENSP00000499852.1:p.Ser373=
ENST00000336642.8:c.170G= ENSP00000338009.4:p.Ser57=
ENST00000345378.6:c.1121G= ENSP00000223366.2:p.Ser374=
ENST00000395796.7:c.1115G= ENSP00000379142.3:p.Ser372=
ENST00000403799.7:c.1118G= ENSP00000384247.3:p.Ser373=
ENST00000437084.1:c.1067G= ENSP00000402840.1:p.Ser356=
ENST00000459642.1:n.498G=
ENST00000616242.4:c.1115G= ENSP00000482149.1:p.Ser372=
NM_000162.3:c.1118G= NP_000153.1:p.Ser373=
NM_033507.1:c.1121G= NP_277042.1:p.Ser374=
NM_033508.1:c.1115G= NP_277043.1:p.Ser372=
NM_000162.4:c.1118G= NP_000153.1:p.Ser373=
NM_001354800.1:c.1118G= NP_001341729.1:p.Ser373=
NM_001354801.1:c.107G= NP_001341730.1:p.Ser36=
NM_001354802.1:c.-23G= NP_001341731.1:n.-23G=
NM_001354803.1:c.152G= NP_001341732.1:p.Ser51=
NM_033507.2:c.1121G= NP_277042.1:p.Ser374=
NM_033508.2:c.1115G= NP_277043.1:p.Ser372=
XM_024446707.1:c.-23G= XP_024302475.1:n.-23G=
NM_000162.5:c.1118G= MANE Select NP_000153.1:p.Ser373=
NM_033507.3:c.1121G= NP_277042.1:p.Ser374=
NM_033508.3:c.1115G= NP_277043.1:p.Ser372=
NM_001354803.2:c.152G= NP_001341732.1:p.Ser51=