Canonical Allele Identifier: CA1703634957
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147826_44147827delinsGC , CM000669.2:g.44147826_44147827delinsGC GRCh38
NC_000007.13:g.44187425_44187426delinsGC , CM000669.1:g.44187425_44187426delinsGC GRCh37
NC_000007.12:g.44153950_44153951delinsGC NCBI36
NG_008847.1:g.46597_46598delinsGC
NG_008847.2:g.55344_55345delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*684_*685delinsGC ENSP00000379142.4:n.*684_*685delinsGC
ENST00000616242.5:c.686_687delinsGC ENSP00000482149.2:p.Gly229=
ENST00000345378.7:c.689_690delinsGC ENSP00000223366.2:p.Gly230=
ENST00000403799.8:c.686_687delinsGC MANE Select ENSP00000384247.3:p.Gly229=
ENST00000671824.1:c.686_687delinsGC ENSP00000500264.1:p.Gly229=
ENST00000673284.1:c.686_687delinsGC ENSP00000499852.1:p.Gly229=
ENST00000345378.6:c.689_690delinsGC ENSP00000223366.2:p.Gly230=
ENST00000395796.7:c.683_684delinsGC ENSP00000379142.3:p.Gly228=
ENST00000403799.7:c.686_687delinsGC ENSP00000384247.3:p.Gly229=
ENST00000437084.1:c.635_636delinsGC ENSP00000402840.1:p.Gly212=
ENST00000616242.4:c.683_684delinsGC ENSP00000482149.1:p.Gly228=
NM_000162.3:c.686_687delinsGC NP_000153.1:p.Gly229=
NM_033507.1:c.689_690delinsGC NP_277042.1:p.Gly230=
NM_033508.1:c.683_684delinsGC NP_277043.1:p.Gly228=
XR_927223.1:n.82+78_82+79delinsGC
NM_000162.4:c.686_687delinsGC NP_000153.1:p.Gly229=
NM_001354800.1:c.686_687delinsGC NP_001341729.1:p.Gly229=
NM_033507.2:c.689_690delinsGC NP_277042.1:p.Gly230=
NM_033508.2:c.683_684delinsGC NP_277043.1:p.Gly228=
XR_927223.2:n.82+78_82+79delinsGC
NM_000162.5:c.686_687delinsGC MANE Select NP_000153.1:p.Gly229=
NM_033507.3:c.689_690delinsGC NP_277042.1:p.Gly230=
NM_033508.3:c.683_684delinsGC NP_277043.1:p.Gly228=