Canonical Allele Identifier: CA618766865

Gene: HEXA

Linked Data

• dbSNP Id: rs1555473007
• gnomAD v2: 15-72645005-ATTT-A
• gnomAD v3: 15-72352664-ATTT-A
• gnomAD v4: 15-72352664-ATTT-A
• MyVariant Identifiers: chr15:g.72645006_72645008del (hg19) ; chr15:g.72352665_72352667del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72352679_72352681del , CM000677.2:g.72352679_72352681del	GRCh38
NC_000015.9:g.72645020_72645022del , CM000677.1:g.72645020_72645022del	GRCh37
NC_000015.8:g.70432074_70432076del	NCBI36
NG_009017.1:g.28513_28515del
NG_009017.2:g.28513_28515del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563908.2:n.2916+401_2916+403del
ENST00000567027.6:c.570+401_570+403del	ENSP00000457521.2:n.570+401_570+403del
ENST00000568260.2:c.590+401_590+403del	ENSP00000458128.2:n.590+401_590+403del
ENST00000682061.1:c.*232+401_*232+403del	ENSP00000508316.1:n.*232+401_*232+403del
ENST00000682177.1:c.570+401_570+403del	ENSP00000507409.1:n.570+401_570+403del
ENST00000682461.1:c.677-1433_677-1431del	ENSP00000507308.1:n.677-1433_677-1431del
ENST00000682653.1:n.601+401_601+403del
ENST00000682657.1:c.254-1433_254-1431del	ENSP00000507753.1:n.254-1433_254-1431del
ENST00000682721.1:c.*373+401_*373+403del	ENSP00000507535.1:n.*373+401_*373+403del
ENST00000682843.1:c.*468+401_*468+403del	ENSP00000508173.1:n.*468+401_*468+403del
ENST00000683003.1:c.413-1433_413-1431del	ENSP00000507576.1:n.413-1433_413-1431del
ENST00000683133.1:c.754+401_754+403del	ENSP00000508108.1:n.754+401_754+403del
ENST00000683228.1:n.601+401_601+403del
ENST00000683243.1:c.413-1433_413-1431del	ENSP00000507042.1:n.413-1433_413-1431del
ENST00000683463.1:c.570+401_570+403del	ENSP00000507986.1:n.570+401_570+403del
ENST00000683548.1:n.601+401_601+403del
ENST00000683579.1:c.*468+401_*468+403del	ENSP00000506867.1:n.*468+401_*468+403del
ENST00000683587.1:n.601+401_601+403del
ENST00000683681.1:c.570+401_570+403del	ENSP00000508110.1:n.570+401_570+403del
ENST00000683735.1:c.*468+401_*468+403del	ENSP00000508336.1:n.*468+401_*468+403del
ENST00000683853.1:c.570+401_570+403del	ENSP00000506834.1:n.570+401_570+403del
ENST00000683860.1:c.570+401_570+403del	ENSP00000507179.1:n.570+401_570+403del
ENST00000683884.1:c.570+401_570+403del	ENSP00000507004.1:n.570+401_570+403del
ENST00000684041.1:c.570+401_570+403del	ENSP00000508382.1:n.570+401_570+403del
ENST00000684125.1:c.570+401_570+403del	ENSP00000507320.1:n.570+401_570+403del
ENST00000684203.1:n.2408+401_2408+403del
ENST00000684231.1:c.413-1433_413-1431del	ENSP00000507748.1:n.413-1433_413-1431del
ENST00000684263.1:c.570+401_570+403del	ENSP00000508369.1:n.570+401_570+403del
ENST00000684305.1:c.1018+401_1018+403del	ENSP00000506819.1:n.1018+401_1018+403del
ENST00000684415.1:c.570+401_570+403del	ENSP00000507227.1:n.570+401_570+403del
ENST00000684520.1:c.570+401_570+403del	ENSP00000506826.1:n.570+401_570+403del
ENST00000684602.1:c.*237-1433_*237-1431del	ENSP00000507996.1:n.*237-1433_*237-1431del
ENST00000684667.1:c.901+401_901+403del	ENSP00000507003.1:n.901+401_901+403del
ENST00000268097.10:c.570+401_570+403del MANE Select	ENSP00000268097.6:n.570+401_570+403del
ENST00000268097.9:c.570+401_570+403del	ENSP00000268097.5:n.570+401_570+403del
ENST00000379915.4:c.412+2892_412+2894del	ENSP00000478716.1:n.412+2892_412+2894del
ENST00000563762.5:c.504-1433_504-1431del	ENSP00000456346.1:n.504-1433_504-1431del
ENST00000566304.5:c.603+401_603+403del	ENSP00000455114.1:n.603+401_603+403del
ENST00000566672.5:c.413-1433_413-1431del	ENSP00000457037.1:n.413-1433_413-1431del
ENST00000567027.5:c.442+401_442+403del
ENST00000567159.5:c.570+401_570+403del	ENSP00000456489.1:n.570+401_570+403del
ENST00000567411.5:c.*91+401_*91+403del	ENSP00000455545.1:n.*91+401_*91+403del
ENST00000568260.1:c.571+401_571+403del
ENST00000568777.5:n.5974+401_5974+403del
ENST00000569410.5:c.570+401_570+403del	ENSP00000457125.1:n.570+401_570+403del
ENST00000569509.5:n.418-1433_418-1431del
NM_000520.4:c.570+401_570+403del	NP_000511.2:n.570+401_570+403del
NM_000520.5:c.570+401_570+403del	NP_000511.2:n.570+401_570+403del
NM_001318825.1:c.603+401_603+403del	NP_001305754.1:n.603+401_603+403del
NR_134869.1:n.1071+401_1071+403del
NM_000520.6:c.570+401_570+403del MANE Select	NP_000511.2:n.570+401_570+403del
NM_001318825.2:c.603+401_603+403del	NP_001305754.1:n.603+401_603+403del
NR_134869.2:n.612+401_612+403del
NR_134869.3:n.612+401_612+403del