Canonical Allele Identifier: CA2186746469

Gene: HEXA

Linked Data

• ClinVar Variation Id: 2916034
• ClinVar RCV Id: RCV003609895
• dbSNP Id: rs1567299267
• gnomAD v4: 15-72353052-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72353052C>T , CM000677.2:g.72353052C>T	GRCh38
NC_000015.9:g.72645393C>T , CM000677.1:g.72645393C>T	GRCh37
NC_000015.8:g.70432447C>T	NCBI36
NG_009017.1:g.28128G>A
NG_009017.2:g.28128G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000563908.2:n.2916+16G>A
ENST00000567027.6:c.570+16G>A	ENSP00000457521.2:n.570+16G>A
ENST00000568260.2:c.590+16G>A	ENSP00000458128.2:n.590+16G>A
ENST00000682061.1:c.*232+16G>A	ENSP00000508316.1:n.*232+16G>A
ENST00000682177.1:c.570+16G>A	ENSP00000507409.1:n.570+16G>A
ENST00000682461.1:c.677-1818G>A	ENSP00000507308.1:n.677-1818G>A
ENST00000682653.1:n.601+16G>A
ENST00000682657.1:c.254-1818G>A	ENSP00000507753.1:n.254-1818G>A
ENST00000682721.1:c.*373+16G>A	ENSP00000507535.1:n.*373+16G>A
ENST00000682843.1:c.*468+16G>A	ENSP00000508173.1:n.*468+16G>A
ENST00000683003.1:c.413-1818G>A	ENSP00000507576.1:n.413-1818G>A
ENST00000683133.1:c.754+16G>A	ENSP00000508108.1:n.754+16G>A
ENST00000683228.1:n.601+16G>A
ENST00000683243.1:c.413-1818G>A	ENSP00000507042.1:n.413-1818G>A
ENST00000683463.1:c.570+16G>A	ENSP00000507986.1:n.570+16G>A
ENST00000683548.1:n.601+16G>A
ENST00000683579.1:c.*468+16G>A	ENSP00000506867.1:n.*468+16G>A
ENST00000683587.1:n.601+16G>A
ENST00000683681.1:c.570+16G>A	ENSP00000508110.1:n.570+16G>A
ENST00000683735.1:c.*468+16G>A	ENSP00000508336.1:n.*468+16G>A
ENST00000683853.1:c.570+16G>A	ENSP00000506834.1:n.570+16G>A
ENST00000683860.1:c.570+16G>A	ENSP00000507179.1:n.570+16G>A
ENST00000683884.1:c.570+16G>A	ENSP00000507004.1:n.570+16G>A
ENST00000684041.1:c.570+16G>A	ENSP00000508382.1:n.570+16G>A
ENST00000684125.1:c.570+16G>A	ENSP00000507320.1:n.570+16G>A
ENST00000684203.1:n.2408+16G>A
ENST00000684231.1:c.413-1818G>A	ENSP00000507748.1:n.413-1818G>A
ENST00000684263.1:c.570+16G>A	ENSP00000508369.1:n.570+16G>A
ENST00000684305.1:c.1018+16G>A	ENSP00000506819.1:n.1018+16G>A
ENST00000684415.1:c.570+16G>A	ENSP00000507227.1:n.570+16G>A
ENST00000684520.1:c.570+16G>A	ENSP00000506826.1:n.570+16G>A
ENST00000684602.1:c.*237-1818G>A	ENSP00000507996.1:n.*237-1818G>A
ENST00000684667.1:c.901+16G>A	ENSP00000507003.1:n.901+16G>A
ENST00000268097.10:c.570+16G>A MANE Select	ENSP00000268097.6:n.570+16G>A
ENST00000268097.9:c.570+16G>A	ENSP00000268097.5:n.570+16G>A
ENST00000379915.4:c.412+2507G>A	ENSP00000478716.1:n.412+2507G>A
ENST00000563762.5:c.504-1818G>A	ENSP00000456346.1:n.504-1818G>A
ENST00000566304.5:c.603+16G>A	ENSP00000455114.1:n.603+16G>A
ENST00000566672.5:c.413-1818G>A	ENSP00000457037.1:n.413-1818G>A
ENST00000567027.5:c.442+16G>A
ENST00000567159.5:c.570+16G>A	ENSP00000456489.1:n.570+16G>A
ENST00000567411.5:c.*91+16G>A	ENSP00000455545.1:n.*91+16G>A
ENST00000568260.1:c.571+16G>A
ENST00000568777.5:n.5974+16G>A
ENST00000569410.5:c.570+16G>A	ENSP00000457125.1:n.570+16G>A
ENST00000569509.5:n.418-1818G>A
NM_000520.4:c.570+16G>A	NP_000511.2:n.570+16G>A
NM_000520.5:c.570+16G>A	NP_000511.2:n.570+16G>A
NM_001318825.1:c.603+16G>A	NP_001305754.1:n.603+16G>A
NR_134869.1:n.1071+16G>A
NM_000520.6:c.570+16G>A MANE Select	NP_000511.2:n.570+16G>A
NM_001318825.2:c.603+16G>A	NP_001305754.1:n.603+16G>A
NR_134869.2:n.612+16G>A
NR_134869.3:n.612+16G>A