Canonical Allele Identifier: CA2186743564
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346283C= , CM000677.2:g.72346283C= GRCh38
NC_000015.9:g.72638624C= , CM000677.1:g.72638624C= GRCh37
NC_000015.8:g.70425678C= NCBI36
NG_009017.1:g.34897G=
NG_009017.2:g.34897G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*33G= ENSP00000457521.2:n.*33G=
ENST00000682061.1:c.*1035G= ENSP00000508316.1:n.*1035G=
ENST00000682064.1:n.916G=
ENST00000682177.1:c.1416G= ENSP00000507409.1:n.1416G=
ENST00000682235.1:n.712G=
ENST00000682461.1:c.1479G= ENSP00000507308.1:n.1479G=
ENST00000682653.1:n.1693G=
ENST00000682657.1:c.*526G= ENSP00000507753.1:n.*526G=
ENST00000682721.1:c.*1176G= ENSP00000507535.1:n.*1176G=
ENST00000682843.1:c.*1014G= ENSP00000508173.1:n.*1014G=
ENST00000683003.1:c.*526G= ENSP00000507576.1:n.*526G=
ENST00000683133.1:c.1557G= ENSP00000508108.1:n.1557G=
ENST00000683243.1:c.*526G= ENSP00000507042.1:n.*526G=
ENST00000683463.1:c.*178G= ENSP00000507986.1:n.*178G=
ENST00000683548.1:n.1147G=
ENST00000683579.1:c.*1271G= ENSP00000506867.1:n.*1271G=
ENST00000683587.1:n.1220G=
ENST00000683681.1:c.1373G= ENSP00000508110.1:p.Cys458=
ENST00000683735.1:c.*1087G= ENSP00000508336.1:n.*1087G=
ENST00000683853.1:c.*178G= ENSP00000506834.1:n.*178G=
ENST00000683860.1:c.1373G= ENSP00000507179.1:p.Cys458=
ENST00000683884.1:c.*16G= ENSP00000507004.1:n.*16G=
ENST00000684041.1:c.1373G= ENSP00000508382.1:p.Cys458=
ENST00000684125.1:c.*33G= ENSP00000507320.1:n.*33G=
ENST00000684203.1:n.3138G=
ENST00000684231.1:c.*783G= ENSP00000507748.1:n.*783G=
ENST00000684263.1:c.*313G= ENSP00000508369.1:n.*313G=
ENST00000684305.1:c.1821G= ENSP00000506819.1:n.1821G=
ENST00000684415.1:c.*240G= ENSP00000507227.1:n.*240G=
ENST00000684520.1:c.1373G= ENSP00000506826.1:p.Cys458=
ENST00000684602.1:c.*1039G= ENSP00000507996.1:n.*1039G=
ENST00000684667.1:c.1704G= ENSP00000507003.1:n.1704G=
ENST00000268097.10:c.1373G= MANE Select ENSP00000268097.6:p.Cys458=
ENST00000268097.9:c.1373G= ENSP00000268097.5:p.Cys458=
ENST00000379915.4:c.455G= ENSP00000478716.1:p.Cys152=
ENST00000563762.5:c.868G= ENSP00000456346.1:n.868G=
ENST00000566304.5:c.1406G= ENSP00000455114.1:p.Cys469=
ENST00000566672.5:c.*783G= ENSP00000457037.1:n.*783G=
ENST00000567027.5:c.988G=
ENST00000567159.5:c.1373G= ENSP00000456489.1:p.Cys458=
ENST00000567411.5:c.*894G= ENSP00000455545.1:n.*894G=
ENST00000568777.5:n.6593G=
ENST00000569410.5:c.*178G= ENSP00000457125.1:n.*178G=
NM_000520.4:c.1373G= NP_000511.2:p.Cys458=
NM_000520.5:c.1373G= NP_000511.2:p.Cys458=
NM_001318825.1:c.1406G= NP_001305754.1:p.Cys469=
NR_134869.1:n.1617G=
NM_000520.6:c.1373G= MANE Select NP_000511.2:p.Cys458=
NM_001318825.2:c.1406G= NP_001305754.1:p.Cys469=
NR_134869.2:n.1158G=
NR_134869.3:n.1158G=