Canonical Allele Identifier: CA2186743341

Gene: HEXA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345671C= , CM000677.2:g.72345671C=	GRCh38
NC_000015.9:g.72638012C= , CM000677.1:g.72638012C=	GRCh37
NC_000015.8:g.70425066C=	NCBI36
NG_009017.1:g.35509G=
NG_009017.2:g.35509G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*82-121G=	ENSP00000457521.2:n.*82-121G=
ENST00000682061.1:c.*1647G=	ENSP00000508316.1:n.*1647G=
ENST00000682064.1:n.1528G=
ENST00000682177.1:c.1465-121G=	ENSP00000507409.1:n.1465-121G=
ENST00000682235.1:n.1324G=
ENST00000682461.1:c.1528-121G=	ENSP00000507308.1:n.1528-121G=
ENST00000682653.1:n.2305G=
ENST00000682657.1:c.*1138G=	ENSP00000507753.1:n.*1138G=
ENST00000682721.1:c.*1225-121G=	ENSP00000507535.1:n.*1225-121G=
ENST00000682843.1:c.*1063-121G=	ENSP00000508173.1:n.*1063-121G=
ENST00000683003.1:c.*1138G=	ENSP00000507576.1:n.*1138G=
ENST00000683133.1:c.1606-121G=	ENSP00000508108.1:n.1606-121G=
ENST00000683243.1:c.*575-121G=	ENSP00000507042.1:n.*575-121G=
ENST00000683463.1:c.*790G=	ENSP00000507986.1:n.*790G=
ENST00000683548.1:n.1759G=
ENST00000683579.1:c.*1320-121G=	ENSP00000506867.1:n.*1320-121G=
ENST00000683587.1:n.1832G=
ENST00000683681.1:c.*99+6G=	ENSP00000508110.1:n.*99+6G=
ENST00000683735.1:c.*1699G=	ENSP00000508336.1:n.*1699G=
ENST00000683853.1:c.*227-121G=	ENSP00000506834.1:n.*227-121G=
ENST00000683860.1:c.*421G=	ENSP00000507179.1:n.*421G=
ENST00000683884.1:c.*628G=	ENSP00000507004.1:n.*628G=
ENST00000684041.1:c.*554+6G=	ENSP00000508382.1:n.*554+6G=
ENST00000684125.1:c.*82-121G=	ENSP00000507320.1:n.*82-121G=
ENST00000684203.1:n.3750G=
ENST00000684231.1:c.*832-121G=	ENSP00000507748.1:n.*832-121G=
ENST00000684263.1:c.*925G=	ENSP00000508369.1:n.*925G=
ENST00000684305.1:c.1870-121G=	ENSP00000506819.1:n.1870-121G=
ENST00000684415.1:c.*852G=	ENSP00000507227.1:n.*852G=
ENST00000684520.1:c.*560G=	ENSP00000506826.1:n.*560G=
ENST00000684602.1:c.*1088-121G=	ENSP00000507996.1:n.*1088-121G=
ENST00000684667.1:c.1753-121G=	ENSP00000507003.1:n.1753-121G=
ENST00000268097.10:c.1422-121G= MANE Select	ENSP00000268097.6:n.1422-121G=
ENST00000268097.9:c.1422-121G=	ENSP00000268097.5:n.1422-121G=
ENST00000379915.4:c.504-121G=	ENSP00000478716.1:n.504-121G=
ENST00000564677.5:n.213+6G=
ENST00000565873.1:n.212G=
ENST00000566304.5:c.1455-121G=	ENSP00000455114.1:n.1455-121G=
ENST00000567027.5:c.1037-121G=
ENST00000567159.5:c.1422-121G=	ENSP00000456489.1:n.1422-121G=
ENST00000567411.5:c.*943-121G=	ENSP00000455545.1:n.*943-121G=
ENST00000568777.5:n.6642-121G=
ENST00000569116.1:n.128+6G=
NM_000520.4:c.1422-121G=	NP_000511.2:n.1422-121G=
NM_000520.5:c.1422-121G=	NP_000511.2:n.1422-121G=
NM_001318825.1:c.1455-121G=	NP_001305754.1:n.1455-121G=
NR_134869.1:n.1666-121G=
NM_000520.6:c.1422-121G= MANE Select	NP_000511.2:n.1422-121G=
NM_001318825.2:c.1455-121G=	NP_001305754.1:n.1455-121G=
NR_134869.2:n.1207-121G=
NR_134869.3:n.1207-121G=