Canonical Allele Identifier: CA2186744885
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72349188T= , CM000677.2:g.72349188T= GRCh38
NC_000015.9:g.72641529T= , CM000677.1:g.72641529T= GRCh37
NC_000015.8:g.70428583T= NCBI36
NG_009017.1:g.31992A=
NG_009017.2:g.31992A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000563908.2:n.3223A=
ENST00000567027.6:c.877A= ENSP00000457521.2:p.Ser293=
ENST00000682061.1:c.*539A= ENSP00000508316.1:n.*539A=
ENST00000682177.1:c.920A= ENSP00000507409.1:n.920A=
ENST00000682461.1:c.983A= ENSP00000507308.1:n.983A=
ENST00000682653.1:n.908A=
ENST00000682657.1:c.*287A= ENSP00000507753.1:n.*287A=
ENST00000682721.1:c.*680A= ENSP00000507535.1:n.*680A=
ENST00000682843.1:c.*775A= ENSP00000508173.1:n.*775A=
ENST00000683003.1:c.*287A= ENSP00000507576.1:n.*287A=
ENST00000683133.1:c.1061A= ENSP00000508108.1:n.1061A=
ENST00000683228.1:n.908A=
ENST00000683243.1:c.*287A= ENSP00000507042.1:n.*287A=
ENST00000683463.1:c.877A= ENSP00000507986.1:p.Ser293=
ENST00000683548.1:n.908A=
ENST00000683579.1:c.*775A= ENSP00000506867.1:n.*775A=
ENST00000683587.1:n.908A=
ENST00000683681.1:c.877A= ENSP00000508110.1:p.Ser293=
ENST00000683735.1:c.*775A= ENSP00000508336.1:n.*775A=
ENST00000683742.1:n.708A=
ENST00000683853.1:c.877A= ENSP00000506834.1:p.Ser293=
ENST00000683860.1:c.877A= ENSP00000507179.1:p.Ser293=
ENST00000683884.1:c.877A= ENSP00000507004.1:p.Ser293=
ENST00000684041.1:c.877A= ENSP00000508382.1:p.Ser293=
ENST00000684125.1:c.877A= ENSP00000507320.1:p.Ser293=
ENST00000684203.1:n.2715A=
ENST00000684231.1:c.*287A= ENSP00000507748.1:n.*287A=
ENST00000684263.1:c.877A= ENSP00000508369.1:p.Ser293=
ENST00000684305.1:c.1325A= ENSP00000506819.1:n.1325A=
ENST00000684415.1:c.877A= ENSP00000507227.1:p.Ser293=
ENST00000684520.1:c.877A= ENSP00000506826.1:p.Ser293=
ENST00000684602.1:c.*543A= ENSP00000507996.1:n.*543A=
ENST00000684667.1:c.1208A= ENSP00000507003.1:n.1208A=
ENST00000268097.10:c.877A= MANE Select ENSP00000268097.6:p.Ser293=
ENST00000268097.9:c.877A= ENSP00000268097.5:p.Ser293=
ENST00000379915.4:c.413-2863A= ENSP00000478716.1:n.413-2863A=
ENST00000563762.5:c.739-1054A= ENSP00000456346.1:n.739-1054A=
ENST00000566304.5:c.910A= ENSP00000455114.1:p.Ser304=
ENST00000566672.5:c.*287A= ENSP00000457037.1:n.*287A=
ENST00000567027.5:c.749A=
ENST00000567159.5:c.877A= ENSP00000456489.1:p.Ser293=
ENST00000567411.5:c.*398A= ENSP00000455545.1:n.*398A=
ENST00000568777.5:n.6281A=
ENST00000569410.5:c.877A= ENSP00000457125.1:p.Ser293=
NM_000520.4:c.877A= NP_000511.2:p.Ser293=
NM_000520.5:c.877A= NP_000511.2:p.Ser293=
NM_001318825.1:c.910A= NP_001305754.1:p.Ser304=
NR_134869.1:n.1378A=
NM_000520.6:c.877A= MANE Select NP_000511.2:p.Ser293=
NM_001318825.2:c.910A= NP_001305754.1:p.Ser304=
NR_134869.2:n.919A=
NR_134869.3:n.919A=