Canonical Allele Identifier: CA1703634923
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147753T= , CM000669.2:g.44147753T= GRCh38
NC_000007.13:g.44187352T= , CM000669.1:g.44187352T= GRCh37
NC_000007.12:g.44153877T= NCBI36
NG_008847.1:g.46671A=
NG_008847.2:g.55418A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*758A= ENSP00000379142.4:n.*758A=
ENST00000616242.5:c.760A= ENSP00000482149.2:p.Asn254=
ENST00000345378.7:c.763A= ENSP00000223366.2:p.Asn255=
ENST00000403799.8:c.760A= MANE Select ENSP00000384247.3:p.Asn254=
ENST00000671824.1:c.760A= ENSP00000500264.1:p.Asn254=
ENST00000673284.1:c.760A= ENSP00000499852.1:p.Asn254=
ENST00000345378.6:c.763A= ENSP00000223366.2:p.Asn255=
ENST00000395796.7:c.757A= ENSP00000379142.3:p.Asn253=
ENST00000403799.7:c.760A= ENSP00000384247.3:p.Asn254=
ENST00000437084.1:c.709A= ENSP00000402840.1:p.Asn237=
ENST00000616242.4:c.757A= ENSP00000482149.1:p.Asn253=
NM_000162.3:c.760A= NP_000153.1:p.Asn254=
NM_033507.1:c.763A= NP_277042.1:p.Asn255=
NM_033508.1:c.757A= NP_277043.1:p.Asn253=
XR_927223.1:n.82+5T=
NM_000162.4:c.760A= NP_000153.1:p.Asn254=
NM_001354800.1:c.760A= NP_001341729.1:p.Asn254=
NM_033507.2:c.763A= NP_277042.1:p.Asn255=
NM_033508.2:c.757A= NP_277043.1:p.Asn253=
XR_927223.2:n.82+5T=
NM_000162.5:c.760A= MANE Select NP_000153.1:p.Asn254=
NM_033507.3:c.763A= NP_277042.1:p.Asn255=
NM_033508.3:c.757A= NP_277043.1:p.Asn253=
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