Canonical Allele Identifier: CA2186743281
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345511G= , CM000677.2:g.72345511G= GRCh38
NC_000015.9:g.72637852G= , CM000677.1:g.72637852G= GRCh37
NC_000015.8:g.70424906G= NCBI36
NG_009017.1:g.35669C=
NG_009017.2:g.35669C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*121C= ENSP00000457521.2:n.*121C=
ENST00000682061.1:c.*1807C= ENSP00000508316.1:n.*1807C=
ENST00000682064.1:n.1688C=
ENST00000682177.1:c.1504C= ENSP00000507409.1:n.1504C=
ENST00000682235.1:n.1484C=
ENST00000682461.1:c.1567C= ENSP00000507308.1:n.1567C=
ENST00000682653.1:n.2465C=
ENST00000682657.1:c.*1298C= ENSP00000507753.1:n.*1298C=
ENST00000682721.1:c.*1264C= ENSP00000507535.1:n.*1264C=
ENST00000682843.1:c.*1102C= ENSP00000508173.1:n.*1102C=
ENST00000683003.1:c.*1298C= ENSP00000507576.1:n.*1298C=
ENST00000683133.1:c.1645C= ENSP00000508108.1:n.1645C=
ENST00000683243.1:c.*614C= ENSP00000507042.1:n.*614C=
ENST00000683463.1:c.*950C= ENSP00000507986.1:n.*950C=
ENST00000683548.1:n.1919C=
ENST00000683579.1:c.*1359C= ENSP00000506867.1:n.*1359C=
ENST00000683587.1:n.1992C=
ENST00000683681.1:c.*139C= ENSP00000508110.1:n.*139C=
ENST00000683735.1:c.*1859C= ENSP00000508336.1:n.*1859C=
ENST00000683853.1:c.*266C= ENSP00000506834.1:n.*266C=
ENST00000683860.1:c.*581C= ENSP00000507179.1:n.*581C=
ENST00000683884.1:c.*788C= ENSP00000507004.1:n.*788C=
ENST00000684041.1:c.*594C= ENSP00000508382.1:n.*594C=
ENST00000684125.1:c.*121C= ENSP00000507320.1:n.*121C=
ENST00000684203.1:n.3910C=
ENST00000684231.1:c.*871C= ENSP00000507748.1:n.*871C=
ENST00000684263.1:c.*1085C= ENSP00000508369.1:n.*1085C=
ENST00000684305.1:c.1909C= ENSP00000506819.1:n.1909C=
ENST00000684415.1:c.*1012C= ENSP00000507227.1:n.*1012C=
ENST00000684520.1:c.*720C= ENSP00000506826.1:n.*720C=
ENST00000684602.1:c.*1127C= ENSP00000507996.1:n.*1127C=
ENST00000684667.1:c.1792C= ENSP00000507003.1:n.1792C=
ENST00000268097.10:c.1461C= MANE Select ENSP00000268097.6:p.Asn487=
ENST00000268097.9:c.1461C= ENSP00000268097.5:p.Asn487=
ENST00000379915.4:c.543C= ENSP00000478716.1:p.Asn181=
ENST00000564677.5:n.253C=
ENST00000565873.1:n.372C=
ENST00000566304.5:c.1494C= ENSP00000455114.1:p.Asn498=
ENST00000567027.5:c.1076C=
ENST00000567159.5:c.1461C= ENSP00000456489.1:p.Asn487=
ENST00000567411.5:c.*982C= ENSP00000455545.1:n.*982C=
ENST00000568777.5:n.6681C=
ENST00000569116.1:n.168C=
NM_000520.4:c.1461C= NP_000511.2:p.Asn487=
NM_000520.5:c.1461C= NP_000511.2:p.Asn487=
NM_001318825.1:c.1494C= NP_001305754.1:p.Asn498=
NR_134869.1:n.1705C=
NM_000520.6:c.1461C= MANE Select NP_000511.2:p.Asn487=
NM_001318825.2:c.1494C= NP_001305754.1:p.Asn498=
NR_134869.2:n.1246C=
NR_134869.3:n.1246C=