Canonical Allele Identifier: CA2695220948
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72347691del , CM000677.2:g.72347691del GRCh38
NC_000015.9:g.72640032del , CM000677.1:g.72640032del GRCh37
NC_000015.8:g.70427086del NCBI36
NG_009017.1:g.33489del
NG_009017.2:g.33489del

Transcript Alleles

HGVS Amino-acid change
ENST00000567027.6:c.1073+357del ENSP00000457521.2:n.1073+357del
ENST00000682061.1:c.*803del ENSP00000508316.1:n.*803del
ENST00000682177.1:c.1184del ENSP00000507409.1:n.1184del
ENST00000682461.1:c.1247del ENSP00000507308.1:n.1247del
ENST00000682653.1:n.1461del
ENST00000682657.1:c.*483+357del ENSP00000507753.1:n.*483+357del
ENST00000682721.1:c.*944del ENSP00000507535.1:n.*944del
ENST00000682843.1:c.*971+357del ENSP00000508173.1:n.*971+357del
ENST00000683003.1:c.*483+357del ENSP00000507576.1:n.*483+357del
ENST00000683133.1:c.1325del ENSP00000508108.1:n.1325del
ENST00000683228.1:n.1172del
ENST00000683243.1:c.*483+357del ENSP00000507042.1:n.*483+357del
ENST00000683463.1:c.1073+357del ENSP00000507986.1:n.1073+357del
ENST00000683548.1:n.1104+357del
ENST00000683579.1:c.*1039del ENSP00000506867.1:n.*1039del
ENST00000683587.1:n.1172del
ENST00000683681.1:c.1141del ENSP00000508110.1:p.Val381Ter
ENST00000683735.1:c.*1039del ENSP00000508336.1:n.*1039del
ENST00000683742.1:n.972del
ENST00000683853.1:c.1073+357del ENSP00000506834.1:n.1073+357del
ENST00000683860.1:c.1141del ENSP00000507179.1:p.Val381Ter
ENST00000683884.1:c.1141del ENSP00000507004.1:p.Val381Ter
ENST00000684041.1:c.1141del ENSP00000508382.1:p.Val381Ter
ENST00000684125.1:c.1073+357del ENSP00000507320.1:n.1073+357del
ENST00000684203.1:n.2911+357del
ENST00000684231.1:c.*551del ENSP00000507748.1:n.*551del
ENST00000684263.1:c.*81del ENSP00000508369.1:n.*81del
ENST00000684305.1:c.1589del ENSP00000506819.1:n.1589del
ENST00000684415.1:c.*13+340del ENSP00000507227.1:n.*13+340del
ENST00000684520.1:c.1141del ENSP00000506826.1:p.Val381Ter
ENST00000684602.1:c.*807del ENSP00000507996.1:n.*807del
ENST00000684667.1:c.1472del ENSP00000507003.1:n.1472del
ENST00000268097.10:c.1141del MANE Select ENSP00000268097.6:p.Val381Ter
ENST00000268097.9:c.1141del ENSP00000268097.5:p.Val381Ter
ENST00000379915.4:c.413-1366del ENSP00000478716.1:n.413-1366del
ENST00000563762.5:c.825+357del ENSP00000456346.1:n.825+357del
ENST00000566304.5:c.1174del ENSP00000455114.1:p.Val392Ter
ENST00000566672.5:c.*551del ENSP00000457037.1:n.*551del
ENST00000567027.5:c.945+357del
ENST00000567159.5:c.1141del ENSP00000456489.1:p.Val381Ter
ENST00000567411.5:c.*662del ENSP00000455545.1:n.*662del
ENST00000568777.5:n.6545del
ENST00000569410.5:c.1073+357del ENSP00000457125.1:n.1073+357del
NM_000520.4:c.1141del NP_000511.2:p.Val381Ter
NM_000520.5:c.1141del NP_000511.2:p.Val381Ter
NM_001318825.1:c.1174del NP_001305754.1:p.Val392Ter
NR_134869.1:n.1574+357del
NM_000520.6:c.1141del MANE Select NP_000511.2:p.Val381Ter
NM_001318825.2:c.1174del NP_001305754.1:p.Val392Ter
NR_134869.2:n.1115+357del
NR_134869.3:n.1115+357del