Canonical Allele Identifier: CA1703634891
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147694A= , CM000669.2:g.44147694A= GRCh38
NC_000007.13:g.44187293A= , CM000669.1:g.44187293A= GRCh37
NC_000007.12:g.44153818A= NCBI36
NG_008847.1:g.46730T=
NG_008847.2:g.55477T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*817T= ENSP00000379142.4:n.*817T=
ENST00000616242.5:c.819T= ENSP00000482149.2:p.Tyr273=
ENST00000345378.7:c.822T= ENSP00000223366.2:p.Tyr274=
ENST00000403799.8:c.819T= MANE Select ENSP00000384247.3:p.Tyr273=
ENST00000671824.1:c.819T= ENSP00000500264.1:p.Tyr273=
ENST00000673284.1:c.819T= ENSP00000499852.1:p.Tyr273=
ENST00000345378.6:c.822T= ENSP00000223366.2:p.Tyr274=
ENST00000395796.7:c.816T= ENSP00000379142.3:p.Tyr272=
ENST00000403799.7:c.819T= ENSP00000384247.3:p.Tyr273=
ENST00000437084.1:c.768T= ENSP00000402840.1:p.Tyr256=
ENST00000616242.4:c.816T= ENSP00000482149.1:p.Tyr272=
NM_000162.3:c.819T= NP_000153.1:p.Tyr273=
NM_033507.1:c.822T= NP_277042.1:p.Tyr274=
NM_033508.1:c.816T= NP_277043.1:p.Tyr272=
XR_927223.1:n.28A=
NM_000162.4:c.819T= NP_000153.1:p.Tyr273=
NM_001354800.1:c.819T= NP_001341729.1:p.Tyr273=
NM_033507.2:c.822T= NP_277042.1:p.Tyr274=
NM_033508.2:c.816T= NP_277043.1:p.Tyr272=
XR_927223.2:n.28A=
NM_000162.5:c.819T= MANE Select NP_000153.1:p.Tyr273=
NM_033507.3:c.822T= NP_277042.1:p.Tyr274=
NM_033508.3:c.816T= NP_277043.1:p.Tyr272=
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