Canonical Allele Identifier: CA2695203086
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147683_44147684delinsCT , CM000669.2:g.44147683_44147684delinsCT GRCh38
NC_000007.13:g.44187282_44187283delinsCT , CM000669.1:g.44187282_44187283delinsCT GRCh37
NC_000007.12:g.44153807_44153808delinsCT NCBI36
NG_008847.1:g.46740_46741delinsAG
NG_008847.2:g.55487_55488delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*827_*828delinsAG ENSP00000379142.4:n.*827_*828delinsAG
ENST00000616242.5:c.829_830delinsAG ENSP00000482149.2:p.Val277Arg
ENST00000345378.7:c.832_833delinsAG ENSP00000223366.2:p.Val278Arg
ENST00000403799.8:c.829_830delinsAG MANE Select ENSP00000384247.3:p.Val277Arg
ENST00000671824.1:c.829_830delinsAG ENSP00000500264.1:p.Val277Arg
ENST00000673284.1:c.829_830delinsAG ENSP00000499852.1:p.Val277Arg
ENST00000345378.6:c.832_833delinsAG ENSP00000223366.2:p.Val278Arg
ENST00000395796.7:c.826_827delinsAG ENSP00000379142.3:p.Val276Arg
ENST00000403799.7:c.829_830delinsAG ENSP00000384247.3:p.Val277Arg
ENST00000437084.1:c.778_779delinsAG ENSP00000402840.1:p.Val260Arg
ENST00000616242.4:c.826_827delinsAG ENSP00000482149.1:p.Val276Arg
NM_000162.3:c.829_830delinsAG NP_000153.1:p.Val277Arg
NM_033507.1:c.832_833delinsAG NP_277042.1:p.Val278Arg
NM_033508.1:c.826_827delinsAG NP_277043.1:p.Val276Arg
XR_927223.1:n.17_18delinsCT
NM_000162.4:c.829_830delinsAG NP_000153.1:p.Val277Arg
NM_001354800.1:c.829_830delinsAG NP_001341729.1:p.Val277Arg
NM_033507.2:c.832_833delinsAG NP_277042.1:p.Val278Arg
NM_033508.2:c.826_827delinsAG NP_277043.1:p.Val276Arg
XR_927223.2:n.17_18delinsCT
NM_000162.5:c.829_830delinsAG MANE Select NP_000153.1:p.Val277Arg
NM_033507.3:c.832_833delinsAG NP_277042.1:p.Val278Arg
NM_033508.3:c.826_827delinsAG NP_277043.1:p.Val276Arg
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