Canonical Allele Identifier: CA2804700380

Gene: HEXA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72352681_72352682insTTTATA , CM000677.2:g.72352681_72352682insTTTATA	GRCh38
NC_000015.9:g.72645022_72645023insTTTATA , CM000677.1:g.72645022_72645023insTTTATA	GRCh37
NC_000015.8:g.70432076_70432077insTTTATA	NCBI36
NG_009017.1:g.28498_28499insTATAAA
NG_009017.2:g.28498_28499insTATAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563908.2:n.2916+386_2916+387insTATAAA
ENST00000567027.6:c.570+386_570+387insTATAAA	ENSP00000457521.2:n.570+386_570+387insTATAAA
ENST00000568260.2:c.590+386_590+387insTATAAA	ENSP00000458128.2:n.590+386_590+387insTATAAA
ENST00000682061.1:c.*232+386_*232+387insTATAAA	ENSP00000508316.1:n.*232+386_*232+387insTATAAA
ENST00000682177.1:c.570+386_570+387insTATAAA	ENSP00000507409.1:n.570+386_570+387insTATAAA
ENST00000682461.1:c.677-1448_677-1447insTATAAA	ENSP00000507308.1:n.677-1448_677-1447insTATAAA
ENST00000682653.1:n.601+386_601+387insTATAAA
ENST00000682657.1:c.254-1448_254-1447insTATAAA	ENSP00000507753.1:n.254-1448_254-1447insTATAAA
ENST00000682721.1:c.*373+386_*373+387insTATAAA	ENSP00000507535.1:n.*373+386_*373+387insTATAAA
ENST00000682843.1:c.*468+386_*468+387insTATAAA	ENSP00000508173.1:n.*468+386_*468+387insTATAAA
ENST00000683003.1:c.413-1448_413-1447insTATAAA	ENSP00000507576.1:n.413-1448_413-1447insTATAAA
ENST00000683133.1:c.754+386_754+387insTATAAA	ENSP00000508108.1:n.754+386_754+387insTATAAA
ENST00000683228.1:n.601+386_601+387insTATAAA
ENST00000683243.1:c.413-1448_413-1447insTATAAA	ENSP00000507042.1:n.413-1448_413-1447insTATAAA
ENST00000683463.1:c.570+386_570+387insTATAAA	ENSP00000507986.1:n.570+386_570+387insTATAAA
ENST00000683548.1:n.601+386_601+387insTATAAA
ENST00000683579.1:c.*468+386_*468+387insTATAAA	ENSP00000506867.1:n.*468+386_*468+387insTATAAA
ENST00000683587.1:n.601+386_601+387insTATAAA
ENST00000683681.1:c.570+386_570+387insTATAAA	ENSP00000508110.1:n.570+386_570+387insTATAAA
ENST00000683735.1:c.*468+386_*468+387insTATAAA	ENSP00000508336.1:n.*468+386_*468+387insTATAAA
ENST00000683853.1:c.570+386_570+387insTATAAA	ENSP00000506834.1:n.570+386_570+387insTATAAA
ENST00000683860.1:c.570+386_570+387insTATAAA	ENSP00000507179.1:n.570+386_570+387insTATAAA
ENST00000683884.1:c.570+386_570+387insTATAAA	ENSP00000507004.1:n.570+386_570+387insTATAAA
ENST00000684041.1:c.570+386_570+387insTATAAA	ENSP00000508382.1:n.570+386_570+387insTATAAA
ENST00000684125.1:c.570+386_570+387insTATAAA	ENSP00000507320.1:n.570+386_570+387insTATAAA
ENST00000684203.1:n.2408+386_2408+387insTATAAA
ENST00000684231.1:c.413-1448_413-1447insTATAAA	ENSP00000507748.1:n.413-1448_413-1447insTATAAA
ENST00000684263.1:c.570+386_570+387insTATAAA	ENSP00000508369.1:n.570+386_570+387insTATAAA
ENST00000684305.1:c.1018+386_1018+387insTATAAA	ENSP00000506819.1:n.1018+386_1018+387insTATAAA
ENST00000684415.1:c.570+386_570+387insTATAAA	ENSP00000507227.1:n.570+386_570+387insTATAAA
ENST00000684520.1:c.570+386_570+387insTATAAA	ENSP00000506826.1:n.570+386_570+387insTATAAA
ENST00000684602.1:c.*237-1448_*237-1447insTATAAA	ENSP00000507996.1:n.*237-1448_*237-1447insTATAAA
ENST00000684667.1:c.901+386_901+387insTATAAA	ENSP00000507003.1:n.901+386_901+387insTATAAA
ENST00000268097.10:c.570+386_570+387insTATAAA MANE Select	ENSP00000268097.6:n.570+386_570+387insTATAAA
ENST00000268097.9:c.570+386_570+387insTATAAA	ENSP00000268097.5:n.570+386_570+387insTATAAA
ENST00000379915.4:c.412+2877_412+2878insTATAAA	ENSP00000478716.1:n.412+2877_412+2878insTATAAA
ENST00000563762.5:c.504-1448_504-1447insTATAAA	ENSP00000456346.1:n.504-1448_504-1447insTATAAA
ENST00000566304.5:c.603+386_603+387insTATAAA	ENSP00000455114.1:n.603+386_603+387insTATAAA
ENST00000566672.5:c.413-1448_413-1447insTATAAA	ENSP00000457037.1:n.413-1448_413-1447insTATAAA
ENST00000567027.5:c.442+386_442+387insTATAAA
ENST00000567159.5:c.570+386_570+387insTATAAA	ENSP00000456489.1:n.570+386_570+387insTATAAA
ENST00000567411.5:c.*91+386_*91+387insTATAAA	ENSP00000455545.1:n.*91+386_*91+387insTATAAA
ENST00000568260.1:c.571+386_571+387insTATAAA
ENST00000568777.5:n.5974+386_5974+387insTATAAA
ENST00000569410.5:c.570+386_570+387insTATAAA	ENSP00000457125.1:n.570+386_570+387insTATAAA
ENST00000569509.5:n.418-1448_418-1447insTATAAA
NM_000520.4:c.570+386_570+387insTATAAA	NP_000511.2:n.570+386_570+387insTATAAA
NM_000520.5:c.570+386_570+387insTATAAA	NP_000511.2:n.570+386_570+387insTATAAA
NM_001318825.1:c.603+386_603+387insTATAAA	NP_001305754.1:n.603+386_603+387insTATAAA
NR_134869.1:n.1071+386_1071+387insTATAAA
NM_000520.6:c.570+386_570+387insTATAAA MANE Select	NP_000511.2:n.570+386_570+387insTATAAA
NM_001318825.2:c.603+386_603+387insTATAAA	NP_001305754.1:n.603+386_603+387insTATAAA
NR_134869.2:n.612+386_612+387insTATAAA
NR_134869.3:n.612+386_612+387insTATAAA