Canonical Allele Identifier: CA2695203083
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147666_44147692del , CM000669.2:g.44147666_44147692del GRCh38
NC_000007.13:g.44187265_44187291del , CM000669.1:g.44187265_44187291del GRCh37
NC_000007.12:g.44153790_44153816del NCBI36
NG_008847.1:g.46735_46761del
NG_008847.2:g.55482_55508del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*822_*848del ENSP00000379142.4:n.*822_*848del
ENST00000616242.5:c.824_850del ENSP00000482149.2:p.Arg275_Asn283del
ENST00000345378.7:c.827_853del ENSP00000223366.2:p.Arg276_Asn284del
ENST00000403799.8:c.824_850del MANE Select ENSP00000384247.3:p.Arg275_Asn283del
ENST00000671824.1:c.824_850del ENSP00000500264.1:p.Arg275_Asn283del
ENST00000673284.1:c.824_850del ENSP00000499852.1:p.Arg275_Asn283del
ENST00000345378.6:c.827_853del ENSP00000223366.2:p.Arg276_Asn284del
ENST00000395796.7:c.821_847del ENSP00000379142.3:p.Arg274_Asn282del
ENST00000403799.7:c.824_850del ENSP00000384247.3:p.Arg275_Asn283del
ENST00000437084.1:c.773_799del ENSP00000402840.1:p.Arg258_Asn266del
ENST00000616242.4:c.821_847del ENSP00000482149.1:p.Arg274_Asn282del
NM_000162.3:c.824_850del NP_000153.1:p.Arg275_Asn283del
NM_033507.1:c.827_853del NP_277042.1:p.Arg276_Asn284del
NM_033508.1:c.821_847del NP_277043.1:p.Arg274_Asn282del
NM_000162.4:c.824_850del NP_000153.1:p.Arg275_Asn283del
NM_001354800.1:c.824_850del NP_001341729.1:p.Arg275_Asn283del
NM_033507.2:c.827_853del NP_277042.1:p.Arg276_Asn284del
NM_033508.2:c.821_847del NP_277043.1:p.Arg274_Asn282del
NM_000162.5:c.824_850del MANE Select NP_000153.1:p.Arg275_Asn283del
NM_033507.3:c.827_853del NP_277042.1:p.Arg276_Asn284del
NM_033508.3:c.821_847del NP_277043.1:p.Arg274_Asn282del
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