Canonical Allele Identifier: CA1703635961
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149977G= , CM000669.2:g.44149977G= GRCh38
NC_000007.13:g.44189576G= , CM000669.1:g.44189576G= GRCh37
NC_000007.12:g.44156101G= NCBI36
NG_008847.1:g.44447C=
NG_008847.2:g.53194C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*569C= ENSP00000379142.4:n.*569C=
ENST00000616242.5:c.571C= ENSP00000482149.2:p.Arg191=
ENST00000682635.1:n.1057C=
ENST00000345378.7:c.574C= ENSP00000223366.2:p.Arg192=
ENST00000403799.8:c.571C= MANE Select ENSP00000384247.3:p.Arg191=
ENST00000671824.1:c.571C= ENSP00000500264.1:p.Arg191=
ENST00000673284.1:c.571C= ENSP00000499852.1:p.Arg191=
ENST00000345378.6:c.574C= ENSP00000223366.2:p.Arg192=
ENST00000395796.7:c.568C= ENSP00000379142.3:p.Arg190=
ENST00000403799.7:c.571C= ENSP00000384247.3:p.Arg191=
ENST00000437084.1:c.520C= ENSP00000402840.1:p.Arg174=
ENST00000616242.4:c.568C= ENSP00000482149.1:p.Arg190=
NM_000162.3:c.571C= NP_000153.1:p.Arg191=
NM_033507.1:c.574C= NP_277042.1:p.Arg192=
NM_033508.1:c.568C= NP_277043.1:p.Arg190=
NM_000162.4:c.571C= NP_000153.1:p.Arg191=
NM_001354800.1:c.571C= NP_001341729.1:p.Arg191=
NM_033507.2:c.574C= NP_277042.1:p.Arg192=
NM_033508.2:c.568C= NP_277043.1:p.Arg190=
NM_000162.5:c.571C= MANE Select NP_000153.1:p.Arg191=
NM_033507.3:c.574C= NP_277042.1:p.Arg192=
NM_033508.3:c.568C= NP_277043.1:p.Arg190=
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