Canonical Allele Identifier: CA2695203094

Gene: GCK

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