Canonical Allele Identifier: CA1703613479
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44146519G= , CM000669.2:g.44146519G= GRCh38
NC_000007.13:g.44186118G= , CM000669.1:g.44186118G= GRCh37
NC_000007.12:g.44152643G= NCBI36
NG_008847.1:g.47905C=
NG_008847.2:g.56652C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*961C= ENSP00000379142.4:n.*961C=
ENST00000616242.5:c.*83C= ENSP00000482149.2:n.*83C=
ENST00000683378.1:n.189C=
ENST00000345378.7:c.966C= ENSP00000223366.2:p.Ser322=
ENST00000403799.8:c.963C= MANE Select ENSP00000384247.3:p.Ser321=
ENST00000671824.1:c.1026C= ENSP00000500264.1:p.Ser342=
ENST00000673284.1:c.963C= ENSP00000499852.1:p.Ser321=
ENST00000345378.6:c.966C= ENSP00000223366.2:p.Ser322=
ENST00000395796.7:c.960C= ENSP00000379142.3:p.Ser320=
ENST00000403799.7:c.963C= ENSP00000384247.3:p.Ser321=
ENST00000437084.1:c.912C= ENSP00000402840.1:p.Ser304=
ENST00000473353.1:n.261C=
ENST00000616242.4:c.960C= ENSP00000482149.1:p.Ser320=
NM_000162.3:c.963C= NP_000153.1:p.Ser321=
NM_033507.1:c.966C= NP_277042.1:p.Ser322=
NM_033508.1:c.960C= NP_277043.1:p.Ser320=
NM_000162.4:c.963C= NP_000153.1:p.Ser321=
NM_001354800.1:c.963C= NP_001341729.1:p.Ser321=
NM_001354801.1:c.8+100C= NP_001341730.1:n.8+100C=
NM_033507.2:c.966C= NP_277042.1:p.Ser322=
NM_033508.2:c.960C= NP_277043.1:p.Ser320=
NM_000162.5:c.963C= MANE Select NP_000153.1:p.Ser321=
NM_033507.3:c.966C= NP_277042.1:p.Ser322=
NM_033508.3:c.960C= NP_277043.1:p.Ser320=