Canonical Allele Identifier: CA2186743312

Gene: HEXA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345588A= , CM000677.2:g.72345588A=	GRCh38
NC_000015.9:g.72637929A= , CM000677.1:g.72637929A=	GRCh37
NC_000015.8:g.70424983A=	NCBI36
NG_009017.1:g.35592T=
NG_009017.2:g.35592T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*82-38T=	ENSP00000457521.2:n.*82-38T=
ENST00000682061.1:c.*1730T=	ENSP00000508316.1:n.*1730T=
ENST00000682064.1:n.1611T=
ENST00000682177.1:c.1465-38T=	ENSP00000507409.1:n.1465-38T=
ENST00000682235.1:n.1407T=
ENST00000682461.1:c.1528-38T=	ENSP00000507308.1:n.1528-38T=
ENST00000682653.1:n.2388T=
ENST00000682657.1:c.*1221T=	ENSP00000507753.1:n.*1221T=
ENST00000682721.1:c.*1225-38T=	ENSP00000507535.1:n.*1225-38T=
ENST00000682843.1:c.*1063-38T=	ENSP00000508173.1:n.*1063-38T=
ENST00000683003.1:c.*1221T=	ENSP00000507576.1:n.*1221T=
ENST00000683133.1:c.1606-38T=	ENSP00000508108.1:n.1606-38T=
ENST00000683243.1:c.*575-38T=	ENSP00000507042.1:n.*575-38T=
ENST00000683463.1:c.*873T=	ENSP00000507986.1:n.*873T=
ENST00000683548.1:n.1842T=
ENST00000683579.1:c.*1320-38T=	ENSP00000506867.1:n.*1320-38T=
ENST00000683587.1:n.1915T=
ENST00000683681.1:c.*100-38T=	ENSP00000508110.1:n.*100-38T=
ENST00000683735.1:c.*1782T=	ENSP00000508336.1:n.*1782T=
ENST00000683853.1:c.*227-38T=	ENSP00000506834.1:n.*227-38T=
ENST00000683860.1:c.*504T=	ENSP00000507179.1:n.*504T=
ENST00000683884.1:c.*711T=	ENSP00000507004.1:n.*711T=
ENST00000684041.1:c.*555-38T=	ENSP00000508382.1:n.*555-38T=
ENST00000684125.1:c.*82-38T=	ENSP00000507320.1:n.*82-38T=
ENST00000684203.1:n.3833T=
ENST00000684231.1:c.*832-38T=	ENSP00000507748.1:n.*832-38T=
ENST00000684263.1:c.*1008T=	ENSP00000508369.1:n.*1008T=
ENST00000684305.1:c.1870-38T=	ENSP00000506819.1:n.1870-38T=
ENST00000684415.1:c.*935T=	ENSP00000507227.1:n.*935T=
ENST00000684520.1:c.*643T=	ENSP00000506826.1:n.*643T=
ENST00000684602.1:c.*1088-38T=	ENSP00000507996.1:n.*1088-38T=
ENST00000684667.1:c.1753-38T=	ENSP00000507003.1:n.1753-38T=
ENST00000268097.10:c.1422-38T= MANE Select	ENSP00000268097.6:n.1422-38T=
ENST00000268097.9:c.1422-38T=	ENSP00000268097.5:n.1422-38T=
ENST00000379915.4:c.504-38T=	ENSP00000478716.1:n.504-38T=
ENST00000564677.5:n.214-38T=
ENST00000565873.1:n.295T=
ENST00000566304.5:c.1455-38T=	ENSP00000455114.1:n.1455-38T=
ENST00000567027.5:c.1037-38T=
ENST00000567159.5:c.1422-38T=	ENSP00000456489.1:n.1422-38T=
ENST00000567411.5:c.*943-38T=	ENSP00000455545.1:n.*943-38T=
ENST00000568777.5:n.6642-38T=
ENST00000569116.1:n.129-38T=
NM_000520.4:c.1422-38T=	NP_000511.2:n.1422-38T=
NM_000520.5:c.1422-38T=	NP_000511.2:n.1422-38T=
NM_001318825.1:c.1455-38T=	NP_001305754.1:n.1455-38T=
NR_134869.1:n.1666-38T=
NM_000520.6:c.1422-38T= MANE Select	NP_000511.2:n.1422-38T=
NM_001318825.2:c.1455-38T=	NP_001305754.1:n.1455-38T=
NR_134869.2:n.1207-38T=
NR_134869.3:n.1207-38T=