Canonical Allele Identifier: CA2629340399

Gene: HEXA

Linked Data

• gnomAD v4: 15-72345667-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345668dup , CM000677.2:g.72345668dup	GRCh38
NC_000015.9:g.72638009dup , CM000677.1:g.72638009dup	GRCh37
NC_000015.8:g.70425063dup	NCBI36
NG_009017.1:g.35512dup
NG_009017.2:g.35512dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*82-118dup	ENSP00000457521.2:n.*82-118dup
ENST00000682061.1:c.*1650dup	ENSP00000508316.1:n.*1650dup
ENST00000682064.1:n.1531dup
ENST00000682177.1:c.1465-118dup	ENSP00000507409.1:n.1465-118dup
ENST00000682235.1:n.1327dup
ENST00000682461.1:c.1528-118dup	ENSP00000507308.1:n.1528-118dup
ENST00000682653.1:n.2308dup
ENST00000682657.1:c.*1141dup	ENSP00000507753.1:n.*1141dup
ENST00000682721.1:c.*1225-118dup	ENSP00000507535.1:n.*1225-118dup
ENST00000682843.1:c.*1063-118dup	ENSP00000508173.1:n.*1063-118dup
ENST00000683003.1:c.*1141dup	ENSP00000507576.1:n.*1141dup
ENST00000683133.1:c.1606-118dup	ENSP00000508108.1:n.1606-118dup
ENST00000683243.1:c.*575-118dup	ENSP00000507042.1:n.*575-118dup
ENST00000683463.1:c.*793dup	ENSP00000507986.1:n.*793dup
ENST00000683548.1:n.1762dup
ENST00000683579.1:c.*1320-118dup	ENSP00000506867.1:n.*1320-118dup
ENST00000683587.1:n.1835dup
ENST00000683681.1:c.*99+9dup	ENSP00000508110.1:n.*99+9dup
ENST00000683735.1:c.*1702dup	ENSP00000508336.1:n.*1702dup
ENST00000683853.1:c.*227-118dup	ENSP00000506834.1:n.*227-118dup
ENST00000683860.1:c.*424dup	ENSP00000507179.1:n.*424dup
ENST00000683884.1:c.*631dup	ENSP00000507004.1:n.*631dup
ENST00000684041.1:c.*554+9dup	ENSP00000508382.1:n.*554+9dup
ENST00000684125.1:c.*82-118dup	ENSP00000507320.1:n.*82-118dup
ENST00000684203.1:n.3753dup
ENST00000684231.1:c.*832-118dup	ENSP00000507748.1:n.*832-118dup
ENST00000684263.1:c.*928dup	ENSP00000508369.1:n.*928dup
ENST00000684305.1:c.1870-118dup	ENSP00000506819.1:n.1870-118dup
ENST00000684415.1:c.*855dup	ENSP00000507227.1:n.*855dup
ENST00000684520.1:c.*563dup	ENSP00000506826.1:n.*563dup
ENST00000684602.1:c.*1088-118dup	ENSP00000507996.1:n.*1088-118dup
ENST00000684667.1:c.1753-118dup	ENSP00000507003.1:n.1753-118dup
ENST00000268097.10:c.1422-118dup MANE Select	ENSP00000268097.6:n.1422-118dup
ENST00000268097.9:c.1422-118dup	ENSP00000268097.5:n.1422-118dup
ENST00000379915.4:c.504-118dup	ENSP00000478716.1:n.504-118dup
ENST00000564677.5:n.213+9dup
ENST00000565873.1:n.215dup
ENST00000566304.5:c.1455-118dup	ENSP00000455114.1:n.1455-118dup
ENST00000567027.5:c.1037-118dup
ENST00000567159.5:c.1422-118dup	ENSP00000456489.1:n.1422-118dup
ENST00000567411.5:c.*943-118dup	ENSP00000455545.1:n.*943-118dup
ENST00000568777.5:n.6642-118dup
ENST00000569116.1:n.128+9dup
NM_000520.4:c.1422-118dup	NP_000511.2:n.1422-118dup
NM_000520.5:c.1422-118dup	NP_000511.2:n.1422-118dup
NM_001318825.1:c.1455-118dup	NP_001305754.1:n.1455-118dup
NR_134869.1:n.1666-118dup
NM_000520.6:c.1422-118dup MANE Select	NP_000511.2:n.1422-118dup
NM_001318825.2:c.1455-118dup	NP_001305754.1:n.1455-118dup
NR_134869.2:n.1207-118dup
NR_134869.3:n.1207-118dup