Canonical Allele Identifier: CA1703634875
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147664_44147665delinsGT , CM000669.2:g.44147664_44147665delinsGT GRCh38
NC_000007.13:g.44187263_44187264delinsGT , CM000669.1:g.44187263_44187264delinsGT GRCh37
NC_000007.12:g.44153788_44153789delinsGT NCBI36
NG_008847.1:g.46759_46760delinsAC
NG_008847.2:g.55506_55507delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*846_*847delinsAC ENSP00000379142.4:n.*846_*847delinsAC
ENST00000616242.5:c.848_849delinsAC ENSP00000482149.2:p.Asn283=
ENST00000345378.7:c.851_852delinsAC ENSP00000223366.2:p.Asn284=
ENST00000403799.8:c.848_849delinsAC MANE Select ENSP00000384247.3:p.Asn283=
ENST00000671824.1:c.848_849delinsAC ENSP00000500264.1:p.Asn283=
ENST00000673284.1:c.848_849delinsAC ENSP00000499852.1:p.Asn283=
ENST00000345378.6:c.851_852delinsAC ENSP00000223366.2:p.Asn284=
ENST00000395796.7:c.845_846delinsAC ENSP00000379142.3:p.Asn282=
ENST00000403799.7:c.848_849delinsAC ENSP00000384247.3:p.Asn283=
ENST00000437084.1:c.797_798delinsAC ENSP00000402840.1:p.Asn266=
ENST00000616242.4:c.845_846delinsAC ENSP00000482149.1:p.Asn282=
NM_000162.3:c.848_849delinsAC NP_000153.1:p.Asn283=
NM_033507.1:c.851_852delinsAC NP_277042.1:p.Asn284=
NM_033508.1:c.845_846delinsAC NP_277043.1:p.Asn282=
NM_000162.4:c.848_849delinsAC NP_000153.1:p.Asn283=
NM_001354800.1:c.848_849delinsAC NP_001341729.1:p.Asn283=
NM_033507.2:c.851_852delinsAC NP_277042.1:p.Asn284=
NM_033508.2:c.845_846delinsAC NP_277043.1:p.Asn282=
NM_000162.5:c.848_849delinsAC MANE Select NP_000153.1:p.Asn283=
NM_033507.3:c.851_852delinsAC NP_277042.1:p.Asn284=
NM_033508.3:c.845_846delinsAC NP_277043.1:p.Asn282=
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