Canonical Allele Identifier: CA2695203094
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147737_44147739del , CM000669.2:g.44147737_44147739del GRCh38
NC_000007.13:g.44187336_44187338del , CM000669.1:g.44187336_44187338del GRCh37
NC_000007.12:g.44153861_44153863del NCBI36
NG_008847.1:g.46686_46688del
NG_008847.2:g.55433_55435del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*773_*775del ENSP00000379142.4:n.*773_*775del
ENST00000616242.5:c.775_777del ENSP00000482149.2:p.Ala259del
ENST00000345378.7:c.778_780del ENSP00000223366.2:p.Ala260del
ENST00000403799.8:c.775_777del MANE Select ENSP00000384247.3:p.Ala259del
ENST00000671824.1:c.775_777del ENSP00000500264.1:p.Ala259del
ENST00000673284.1:c.775_777del ENSP00000499852.1:p.Ala259del
ENST00000345378.6:c.778_780del ENSP00000223366.2:p.Ala260del
ENST00000395796.7:c.772_774del ENSP00000379142.3:p.Ala258del
ENST00000403799.7:c.775_777del ENSP00000384247.3:p.Ala259del
ENST00000437084.1:c.724_726del ENSP00000402840.1:p.Ala242del
ENST00000616242.4:c.772_774del ENSP00000482149.1:p.Ala258del
NM_000162.3:c.775_777del NP_000153.1:p.Ala259del
NM_033507.1:c.778_780del NP_277042.1:p.Ala260del
NM_033508.1:c.772_774del NP_277043.1:p.Ala258del
XR_927223.1:n.71_73del
NM_000162.4:c.775_777del NP_000153.1:p.Ala259del
NM_001354800.1:c.775_777del NP_001341729.1:p.Ala259del
NM_033507.2:c.778_780del NP_277042.1:p.Ala260del
NM_033508.2:c.772_774del NP_277043.1:p.Ala258del
XR_927223.2:n.71_73del
NM_000162.5:c.775_777del MANE Select NP_000153.1:p.Ala259del
NM_033507.3:c.778_780del NP_277042.1:p.Ala260del
NM_033508.3:c.772_774del NP_277043.1:p.Ala258del
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