Canonical Allele Identifier: CA971330868
Gene: HEXA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72347271_72347274del , CM000677.2:g.72347271_72347274del GRCh38
NC_000015.9:g.72639612_72639615del , CM000677.1:g.72639612_72639615del GRCh37
NC_000015.8:g.70426666_70426669del NCBI36
NG_009017.1:g.33906_33909del
NG_009017.2:g.33906_33909del

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.1073+774_1073+777del ENSP00000457521.2:n.1073+774_1073+777del
ENST00000682061.1:c.*808+412_*808+415del ENSP00000508316.1:n.*808+412_*808+415del
ENST00000682177.1:c.1189+412_1189+415del ENSP00000507409.1:n.1189+412_1189+415del
ENST00000682461.1:c.1252+412_1252+415del ENSP00000507308.1:n.1252+412_1252+415del
ENST00000682653.1:n.1466+412_1466+415del
ENST00000682657.1:c.*483+774_*483+777del ENSP00000507753.1:n.*483+774_*483+777del
ENST00000682721.1:c.*949+412_*949+415del ENSP00000507535.1:n.*949+412_*949+415del
ENST00000682843.1:c.*971+774_*971+777del ENSP00000508173.1:n.*971+774_*971+777del
ENST00000683003.1:c.*483+774_*483+777del ENSP00000507576.1:n.*483+774_*483+777del
ENST00000683133.1:c.1330+412_1330+415del ENSP00000508108.1:n.1330+412_1330+415del
ENST00000683228.1:n.1589_1592del
ENST00000683243.1:c.*483+774_*483+777del ENSP00000507042.1:n.*483+774_*483+777del
ENST00000683463.1:c.1074-564_1074-561del ENSP00000507986.1:n.1074-564_1074-561del
ENST00000683548.1:n.1104+774_1104+777del
ENST00000683579.1:c.*1044+412_*1044+415del ENSP00000506867.1:n.*1044+412_*1044+415del
ENST00000683587.1:n.1177+412_1177+415del
ENST00000683681.1:c.1146+412_1146+415del ENSP00000508110.1:n.1146+412_1146+415del
ENST00000683735.1:c.*1044+412_*1044+415del ENSP00000508336.1:n.*1044+412_*1044+415del
ENST00000683742.1:n.1389_1392del
ENST00000683853.1:c.1074-564_1074-561del ENSP00000506834.1:n.1074-564_1074-561del
ENST00000683860.1:c.1146+412_1146+415del ENSP00000507179.1:n.1146+412_1146+415del
ENST00000683884.1:c.1146+412_1146+415del ENSP00000507004.1:n.1146+412_1146+415del
ENST00000684041.1:c.1146+412_1146+415del ENSP00000508382.1:n.1146+412_1146+415del
ENST00000684125.1:c.1073+774_1073+777del ENSP00000507320.1:n.1073+774_1073+777del
ENST00000684203.1:n.2912-564_2912-561del
ENST00000684231.1:c.*556+412_*556+415del ENSP00000507748.1:n.*556+412_*556+415del
ENST00000684263.1:c.*86+412_*86+415del ENSP00000508369.1:n.*86+412_*86+415del
ENST00000684305.1:c.1594+412_1594+415del ENSP00000506819.1:n.1594+412_1594+415del
ENST00000684415.1:c.*14-564_*14-561del ENSP00000507227.1:n.*14-564_*14-561del
ENST00000684520.1:c.1146+412_1146+415del ENSP00000506826.1:n.1146+412_1146+415del
ENST00000684602.1:c.*812+412_*812+415del ENSP00000507996.1:n.*812+412_*812+415del
ENST00000684667.1:c.1477+412_1477+415del ENSP00000507003.1:n.1477+412_1477+415del
ENST00000268097.10:c.1146+412_1146+415del MANE Select ENSP00000268097.6:n.1146+412_1146+415del
ENST00000268097.9:c.1146+412_1146+415del ENSP00000268097.5:n.1146+412_1146+415del
ENST00000379915.4:c.413-949_413-946del ENSP00000478716.1:n.413-949_413-946del
ENST00000563762.5:c.825+774_825+777del ENSP00000456346.1:n.825+774_825+777del
ENST00000566304.5:c.1179+412_1179+415del ENSP00000455114.1:n.1179+412_1179+415del
ENST00000566672.5:c.*556+412_*556+415del ENSP00000457037.1:n.*556+412_*556+415del
ENST00000567027.5:c.945+774_945+777del
ENST00000567159.5:c.1146+412_1146+415del ENSP00000456489.1:n.1146+412_1146+415del
ENST00000567411.5:c.*667+412_*667+415del ENSP00000455545.1:n.*667+412_*667+415del
ENST00000568777.5:n.6550+412_6550+415del
ENST00000569410.5:c.1074-564_1074-561del ENSP00000457125.1:n.1074-564_1074-561del
NM_000520.4:c.1146+412_1146+415del NP_000511.2:n.1146+412_1146+415del
NM_000520.5:c.1146+412_1146+415del NP_000511.2:n.1146+412_1146+415del
NM_001318825.1:c.1179+412_1179+415del NP_001305754.1:n.1179+412_1179+415del
NR_134869.1:n.1574+774_1574+777del
NM_000520.6:c.1146+412_1146+415del MANE Select NP_000511.2:n.1146+412_1146+415del
NM_001318825.2:c.1179+412_1179+415del NP_001305754.1:n.1179+412_1179+415del
NR_134869.2:n.1115+774_1115+777del
NR_134869.3:n.1115+774_1115+777del