Canonical Allele Identifier: CA2697549194

Gene: HEXA

Linked Data

• ClinVar Variation Id: 2712729
• ClinVar RCV Id: RCV003503795

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72348109del , CM000677.2:g.72348109del	GRCh38
NC_000015.9:g.72640450del , CM000677.1:g.72640450del	GRCh37
NC_000015.8:g.70427504del	NCBI36
NG_009017.1:g.33073del
NG_009017.2:g.33073del

Transcript Alleles

HGVS	Amino-acid change
ENST00000563908.2:n.3360del
ENST00000567027.6:c.1014del	ENSP00000457521.2:p.Phe338LeufsTer2
ENST00000682061.1:c.*676del	ENSP00000508316.1:n.*676del
ENST00000682177.1:c.1057del	ENSP00000507409.1:n.1057del
ENST00000682461.1:c.1120del	ENSP00000507308.1:n.1120del
ENST00000682653.1:n.1045del
ENST00000682657.1:c.*424del	ENSP00000507753.1:n.*424del
ENST00000682721.1:c.*817del	ENSP00000507535.1:n.*817del
ENST00000682843.1:c.*912del	ENSP00000508173.1:n.*912del
ENST00000683003.1:c.*424del	ENSP00000507576.1:n.*424del
ENST00000683133.1:c.1198del	ENSP00000508108.1:n.1198del
ENST00000683228.1:n.1045del
ENST00000683243.1:c.*424del	ENSP00000507042.1:n.*424del
ENST00000683463.1:c.1014del	ENSP00000507986.1:p.Phe338LeufsTer2
ENST00000683548.1:n.1045del
ENST00000683579.1:c.*912del	ENSP00000506867.1:n.*912del
ENST00000683587.1:n.1045del
ENST00000683681.1:c.1014del	ENSP00000508110.1:p.Phe338LeufsTer2
ENST00000683735.1:c.*912del	ENSP00000508336.1:n.*912del
ENST00000683742.1:n.845del
ENST00000683853.1:c.1014del	ENSP00000506834.1:p.Phe338LeufsTer2
ENST00000683860.1:c.1014del	ENSP00000507179.1:p.Phe338LeufsTer2
ENST00000683884.1:c.1014del	ENSP00000507004.1:p.Phe338LeufsTer2
ENST00000684041.1:c.1014del	ENSP00000508382.1:p.Phe338LeufsTer2
ENST00000684125.1:c.1014del	ENSP00000507320.1:p.Phe338LeufsTer2
ENST00000684203.1:n.2852del
ENST00000684231.1:c.*424del	ENSP00000507748.1:n.*424del
ENST00000684263.1:c.1014del	ENSP00000508369.1:p.Phe338LeufsTer2
ENST00000684305.1:c.1462del	ENSP00000506819.1:n.1462del
ENST00000684415.1:c.1014del	ENSP00000507227.1:p.Phe338LeufsTer2
ENST00000684520.1:c.1014del	ENSP00000506826.1:p.Phe338LeufsTer2
ENST00000684602.1:c.*680del	ENSP00000507996.1:n.*680del
ENST00000684667.1:c.1345del	ENSP00000507003.1:n.1345del
ENST00000268097.10:c.1014del MANE Select	ENSP00000268097.6:p.Phe338LeufsTer2
ENST00000268097.9:c.1014del	ENSP00000268097.5:p.Phe338LeufsTer2
ENST00000379915.4:c.413-1782del	ENSP00000478716.1:n.413-1782del
ENST00000563762.5:c.766del	ENSP00000456346.1:n.766del
ENST00000566304.5:c.1047del	ENSP00000455114.1:p.Phe349LeufsTer2
ENST00000566672.5:c.*424del	ENSP00000457037.1:n.*424del
ENST00000567027.5:c.886del
ENST00000567159.5:c.1014del	ENSP00000456489.1:p.Phe338LeufsTer2
ENST00000567411.5:c.*535del	ENSP00000455545.1:n.*535del
ENST00000568777.5:n.6418del
ENST00000569410.5:c.1014del	ENSP00000457125.1:p.Phe338LeufsTer2
NM_000520.4:c.1014del	NP_000511.2:p.Phe338LeufsTer2
NM_000520.5:c.1014del	NP_000511.2:p.Phe338LeufsTer2
NM_001318825.1:c.1047del	NP_001305754.1:p.Phe349LeufsTer2
NR_134869.1:n.1515del
NM_000520.6:c.1014del MANE Select	NP_000511.2:p.Phe338LeufsTer2
NM_001318825.2:c.1047del	NP_001305754.1:p.Phe349LeufsTer2
NR_134869.2:n.1056del
NR_134869.3:n.1056del