Canonical Allele Identifier: CA7644828
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 1406911
ClinVar RCV Id: RCV001918169
dbSNP Id: rs780502991

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72348044T>C , CM000677.2:g.72348044T>C GRCh38
NC_000015.9:g.72640385T>C , CM000677.1:g.72640385T>C GRCh37
NC_000015.8:g.70427439T>C NCBI36
NG_009017.1:g.33136A>G
NG_009017.2:g.33136A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000563908.2:n.3423A>G
ENST00000567027.6:c.1073+4A>G ENSP00000457521.2:n.1073+4A>G
ENST00000682061.1:c.*735+4A>G ENSP00000508316.1:n.*735+4A>G
ENST00000682177.1:c.1116+4A>G ENSP00000507409.1:n.1116+4A>G
ENST00000682461.1:c.1179+4A>G ENSP00000507308.1:n.1179+4A>G
ENST00000682653.1:n.1108A>G
ENST00000682657.1:c.*483+4A>G ENSP00000507753.1:n.*483+4A>G
ENST00000682721.1:c.*876+4A>G ENSP00000507535.1:n.*876+4A>G
ENST00000682843.1:c.*971+4A>G ENSP00000508173.1:n.*971+4A>G
ENST00000683003.1:c.*483+4A>G ENSP00000507576.1:n.*483+4A>G
ENST00000683133.1:c.1257+4A>G ENSP00000508108.1:n.1257+4A>G
ENST00000683228.1:n.1104+4A>G
ENST00000683243.1:c.*483+4A>G ENSP00000507042.1:n.*483+4A>G
ENST00000683463.1:c.1073+4A>G ENSP00000507986.1:n.1073+4A>G
ENST00000683548.1:n.1104+4A>G
ENST00000683579.1:c.*971+4A>G ENSP00000506867.1:n.*971+4A>G
ENST00000683587.1:n.1104+4A>G
ENST00000683681.1:c.1073+4A>G ENSP00000508110.1:n.1073+4A>G
ENST00000683735.1:c.*971+4A>G ENSP00000508336.1:n.*971+4A>G
ENST00000683742.1:n.904+4A>G
ENST00000683853.1:c.1073+4A>G ENSP00000506834.1:n.1073+4A>G
ENST00000683860.1:c.1073+4A>G ENSP00000507179.1:n.1073+4A>G
ENST00000683884.1:c.1073+4A>G ENSP00000507004.1:n.1073+4A>G
ENST00000684041.1:c.1073+4A>G ENSP00000508382.1:n.1073+4A>G
ENST00000684125.1:c.1073+4A>G ENSP00000507320.1:n.1073+4A>G
ENST00000684203.1:n.2911+4A>G
ENST00000684231.1:c.*483+4A>G ENSP00000507748.1:n.*483+4A>G
ENST00000684263.1:c.1077A>G ENSP00000508369.1:p.Ter359Trp
ENST00000684305.1:c.1521+4A>G ENSP00000506819.1:n.1521+4A>G
ENST00000684415.1:c.1077A>G ENSP00000507227.1:p.Ter359Trp
ENST00000684520.1:c.1073+4A>G ENSP00000506826.1:n.1073+4A>G
ENST00000684602.1:c.*739+4A>G ENSP00000507996.1:n.*739+4A>G
ENST00000684667.1:c.1404+4A>G ENSP00000507003.1:n.1404+4A>G
ENST00000268097.10:c.1073+4A>G MANE Select ENSP00000268097.6:n.1073+4A>G
ENST00000268097.9:c.1073+4A>G ENSP00000268097.5:n.1073+4A>G
ENST00000379915.4:c.413-1719A>G ENSP00000478716.1:n.413-1719A>G
ENST00000563762.5:c.825+4A>G ENSP00000456346.1:n.825+4A>G
ENST00000566304.5:c.1106+4A>G ENSP00000455114.1:n.1106+4A>G
ENST00000566672.5:c.*483+4A>G ENSP00000457037.1:n.*483+4A>G
ENST00000567027.5:c.945+4A>G
ENST00000567159.5:c.1073+4A>G ENSP00000456489.1:n.1073+4A>G
ENST00000567411.5:c.*594+4A>G ENSP00000455545.1:n.*594+4A>G
ENST00000568777.5:n.6477+4A>G
ENST00000569410.5:c.1073+4A>G ENSP00000457125.1:n.1073+4A>G
NM_000520.4:c.1073+4A>G NP_000511.2:n.1073+4A>G
NM_000520.5:c.1073+4A>G NP_000511.2:n.1073+4A>G
NM_001318825.1:c.1106+4A>G NP_001305754.1:n.1106+4A>G
NR_134869.1:n.1574+4A>G
NM_000520.6:c.1073+4A>G MANE Select NP_000511.2:n.1073+4A>G
NM_001318825.2:c.1106+4A>G NP_001305754.1:n.1106+4A>G
NR_134869.2:n.1115+4A>G
NR_134869.3:n.1115+4A>G