Canonical Allele Identifier: CA2186746262
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72352594_72352596delinsCTG , CM000677.2:g.72352594_72352596delinsCTG GRCh38
NC_000015.9:g.72644935_72644937delinsCTG , CM000677.1:g.72644935_72644937delinsCTG GRCh37
NC_000015.8:g.70431989_70431991delinsCTG NCBI36
NG_009017.1:g.28584_28586delinsCAG
NG_009017.2:g.28584_28586delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000563908.2:n.2916+472_2916+474delinsCAG
ENST00000567027.6:c.570+472_570+474delinsCAG ENSP00000457521.2:n.570+472_570+474delinsCAG
ENST00000568260.2:c.590+472_590+474delinsCAG ENSP00000458128.2:n.590+472_590+474delinsCAG
ENST00000682061.1:c.*232+472_*232+474delinsCAG ENSP00000508316.1:n.*232+472_*232+474delinsCAG
ENST00000682177.1:c.570+472_570+474delinsCAG ENSP00000507409.1:n.570+472_570+474delinsCAG
ENST00000682461.1:c.677-1362_677-1360delinsCAG ENSP00000507308.1:n.677-1362_677-1360delinsCAG
ENST00000682653.1:n.601+472_601+474delinsCAG
ENST00000682657.1:c.254-1362_254-1360delinsCAG ENSP00000507753.1:n.254-1362_254-1360delinsCAG
ENST00000682721.1:c.*373+472_*373+474delinsCAG ENSP00000507535.1:n.*373+472_*373+474delinsCAG
ENST00000682843.1:c.*468+472_*468+474delinsCAG ENSP00000508173.1:n.*468+472_*468+474delinsCAG
ENST00000683003.1:c.413-1362_413-1360delinsCAG ENSP00000507576.1:n.413-1362_413-1360delinsCAG
ENST00000683133.1:c.754+472_754+474delinsCAG ENSP00000508108.1:n.754+472_754+474delinsCAG
ENST00000683228.1:n.601+472_601+474delinsCAG
ENST00000683243.1:c.413-1362_413-1360delinsCAG ENSP00000507042.1:n.413-1362_413-1360delinsCAG
ENST00000683463.1:c.570+472_570+474delinsCAG ENSP00000507986.1:n.570+472_570+474delinsCAG
ENST00000683548.1:n.601+472_601+474delinsCAG
ENST00000683579.1:c.*468+472_*468+474delinsCAG ENSP00000506867.1:n.*468+472_*468+474delinsCAG
ENST00000683587.1:n.601+472_601+474delinsCAG
ENST00000683681.1:c.570+472_570+474delinsCAG ENSP00000508110.1:n.570+472_570+474delinsCAG
ENST00000683735.1:c.*468+472_*468+474delinsCAG ENSP00000508336.1:n.*468+472_*468+474delinsCAG
ENST00000683853.1:c.570+472_570+474delinsCAG ENSP00000506834.1:n.570+472_570+474delinsCAG
ENST00000683860.1:c.570+472_570+474delinsCAG ENSP00000507179.1:n.570+472_570+474delinsCAG
ENST00000683884.1:c.570+472_570+474delinsCAG ENSP00000507004.1:n.570+472_570+474delinsCAG
ENST00000684041.1:c.570+472_570+474delinsCAG ENSP00000508382.1:n.570+472_570+474delinsCAG
ENST00000684125.1:c.570+472_570+474delinsCAG ENSP00000507320.1:n.570+472_570+474delinsCAG
ENST00000684203.1:n.2408+472_2408+474delinsCAG
ENST00000684231.1:c.413-1362_413-1360delinsCAG ENSP00000507748.1:n.413-1362_413-1360delinsCAG
ENST00000684263.1:c.570+472_570+474delinsCAG ENSP00000508369.1:n.570+472_570+474delinsCAG
ENST00000684305.1:c.1018+472_1018+474delinsCAG ENSP00000506819.1:n.1018+472_1018+474delinsCAG
ENST00000684415.1:c.570+472_570+474delinsCAG ENSP00000507227.1:n.570+472_570+474delinsCAG
ENST00000684520.1:c.570+472_570+474delinsCAG ENSP00000506826.1:n.570+472_570+474delinsCAG
ENST00000684602.1:c.*237-1362_*237-1360delinsCAG ENSP00000507996.1:n.*237-1362_*237-1360delinsCAG
ENST00000684667.1:c.901+472_901+474delinsCAG ENSP00000507003.1:n.901+472_901+474delinsCAG
ENST00000268097.10:c.570+472_570+474delinsCAG MANE Select ENSP00000268097.6:n.570+472_570+474delinsCAG
ENST00000268097.9:c.570+472_570+474delinsCAG ENSP00000268097.5:n.570+472_570+474delinsCAG
ENST00000379915.4:c.412+2963_412+2965delinsCAG ENSP00000478716.1:n.412+2963_412+2965delinsCAG
ENST00000563762.5:c.504-1362_504-1360delinsCAG ENSP00000456346.1:n.504-1362_504-1360delinsCAG
ENST00000566304.5:c.603+472_603+474delinsCAG ENSP00000455114.1:n.603+472_603+474delinsCAG
ENST00000566672.5:c.413-1362_413-1360delinsCAG ENSP00000457037.1:n.413-1362_413-1360delinsCAG
ENST00000567027.5:c.442+472_442+474delinsCAG
ENST00000567159.5:c.570+472_570+474delinsCAG ENSP00000456489.1:n.570+472_570+474delinsCAG
ENST00000567411.5:c.*91+472_*91+474delinsCAG ENSP00000455545.1:n.*91+472_*91+474delinsCAG
ENST00000568260.1:c.571+472_571+474delinsCAG
ENST00000568777.5:n.5974+472_5974+474delinsCAG
ENST00000569410.5:c.570+472_570+474delinsCAG ENSP00000457125.1:n.570+472_570+474delinsCAG
ENST00000569509.5:n.418-1362_418-1360delinsCAG
NM_000520.4:c.570+472_570+474delinsCAG NP_000511.2:n.570+472_570+474delinsCAG
NM_000520.5:c.570+472_570+474delinsCAG NP_000511.2:n.570+472_570+474delinsCAG
NM_001318825.1:c.603+472_603+474delinsCAG NP_001305754.1:n.603+472_603+474delinsCAG
NR_134869.1:n.1071+472_1071+474delinsCAG
NM_000520.6:c.570+472_570+474delinsCAG MANE Select NP_000511.2:n.570+472_570+474delinsCAG
NM_001318825.2:c.603+472_603+474delinsCAG NP_001305754.1:n.603+472_603+474delinsCAG
NR_134869.2:n.612+472_612+474delinsCAG
NR_134869.3:n.612+472_612+474delinsCAG