Canonical Allele Identifier: CA16044208
Gene: HEXA HGNC NCBI

Linked Data

ClinVar Variation Id: 375353
ClinVar RCV Id: RCV000416473
dbSNP Id: rs1057519460

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72353114T>G , CM000677.2:g.72353114T>G GRCh38
NC_000015.9:g.72645455T>G , CM000677.1:g.72645455T>G GRCh37
NC_000015.8:g.70432509T>G NCBI36
NG_009017.1:g.28066A>C
NG_009017.2:g.28066A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000563908.2:n.2870A>C
ENST00000567027.6:c.524A>C ENSP00000457521.2:p.Asp175Ala
ENST00000568260.2:c.544A>C ENSP00000458128.2:n.544A>C
ENST00000682061.1:c.*186A>C ENSP00000508316.1:n.*186A>C
ENST00000682177.1:c.524A>C ENSP00000507409.1:p.Asp175Ala
ENST00000682461.1:c.677-1880A>C ENSP00000507308.1:n.677-1880A>C
ENST00000682653.1:n.555A>C
ENST00000682657.1:c.254-1880A>C ENSP00000507753.1:n.254-1880A>C
ENST00000682721.1:c.*327A>C ENSP00000507535.1:n.*327A>C
ENST00000682843.1:c.*422A>C ENSP00000508173.1:n.*422A>C
ENST00000683003.1:c.413-1880A>C ENSP00000507576.1:n.413-1880A>C
ENST00000683133.1:c.708A>C ENSP00000508108.1:n.708A>C
ENST00000683228.1:n.555A>C
ENST00000683243.1:c.413-1880A>C ENSP00000507042.1:n.413-1880A>C
ENST00000683463.1:c.524A>C ENSP00000507986.1:p.Asp175Ala
ENST00000683548.1:n.555A>C
ENST00000683579.1:c.*422A>C ENSP00000506867.1:n.*422A>C
ENST00000683587.1:n.555A>C
ENST00000683681.1:c.524A>C ENSP00000508110.1:p.Asp175Ala
ENST00000683735.1:c.*422A>C ENSP00000508336.1:n.*422A>C
ENST00000683853.1:c.524A>C ENSP00000506834.1:p.Asp175Ala
ENST00000683860.1:c.524A>C ENSP00000507179.1:p.Asp175Ala
ENST00000683884.1:c.524A>C ENSP00000507004.1:p.Asp175Ala
ENST00000684041.1:c.524A>C ENSP00000508382.1:p.Asp175Ala
ENST00000684125.1:c.524A>C ENSP00000507320.1:p.Asp175Ala
ENST00000684203.1:n.2362A>C
ENST00000684231.1:c.413-1880A>C ENSP00000507748.1:n.413-1880A>C
ENST00000684263.1:c.524A>C ENSP00000508369.1:p.Asp175Ala
ENST00000684305.1:c.972A>C ENSP00000506819.1:n.972A>C
ENST00000684415.1:c.524A>C ENSP00000507227.1:p.Asp175Ala
ENST00000684520.1:c.524A>C ENSP00000506826.1:p.Asp175Ala
ENST00000684602.1:c.*237-1880A>C ENSP00000507996.1:n.*237-1880A>C
ENST00000684667.1:c.855A>C ENSP00000507003.1:n.855A>C
ENST00000268097.10:c.524A>C MANE Select ENSP00000268097.6:p.Asp175Ala
ENST00000268097.9:c.524A>C ENSP00000268097.5:p.Asp175Ala
ENST00000379915.4:c.412+2445A>C ENSP00000478716.1:n.412+2445A>C
ENST00000563762.5:c.504-1880A>C ENSP00000456346.1:n.504-1880A>C
ENST00000566304.5:c.557A>C ENSP00000455114.1:p.Asp186Ala
ENST00000566672.5:c.413-1880A>C ENSP00000457037.1:n.413-1880A>C
ENST00000567027.5:c.396A>C
ENST00000567159.5:c.524A>C ENSP00000456489.1:p.Asp175Ala
ENST00000567411.5:c.*45A>C ENSP00000455545.1:n.*45A>C
ENST00000568260.1:c.525A>C
ENST00000568777.5:n.5928A>C
ENST00000569410.5:c.524A>C ENSP00000457125.1:p.Asp175Ala
ENST00000569509.5:n.418-1880A>C
NM_000520.4:c.524A>C NP_000511.2:p.Asp175Ala
NM_000520.5:c.524A>C NP_000511.2:p.Asp175Ala
NM_001318825.1:c.557A>C NP_001305754.1:p.Asp186Ala
NR_134869.1:n.1025A>C
NM_000520.6:c.524A>C MANE Select NP_000511.2:p.Asp175Ala
NM_001318825.2:c.557A>C NP_001305754.1:p.Asp186Ala
NR_134869.2:n.566A>C
NR_134869.3:n.566A>C