Canonical Allele Identifier: CA2186743113

Gene: HEXA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345187C= , CM000677.2:g.72345187C=	GRCh38
NC_000015.9:g.72637528C= , CM000677.1:g.72637528C=	GRCh37
NC_000015.8:g.70424582C=	NCBI36
NG_009017.1:g.35993G=
NG_009017.2:g.35993G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682064.1:n.1753+259G=
ENST00000682235.1:n.1549+259G=
ENST00000682461.1:c.1632+259G=	ENSP00000507308.1:n.1632+259G=
ENST00000682653.1:n.2789G=
ENST00000682721.1:c.*1329+259G=	ENSP00000507535.1:n.*1329+259G=
ENST00000682843.1:c.*1167+259G=	ENSP00000508173.1:n.*1167+259G=
ENST00000683133.1:c.1710+259G=	ENSP00000508108.1:n.1710+259G=
ENST00000683243.1:c.*679+259G=	ENSP00000507042.1:n.*679+259G=
ENST00000683463.1:c.*1015+259G=	ENSP00000507986.1:n.*1015+259G=
ENST00000683548.1:n.1984+259G=
ENST00000683579.1:c.*1424+259G=	ENSP00000506867.1:n.*1424+259G=
ENST00000683587.1:n.2057+259G=
ENST00000683681.1:c.*204+259G=	ENSP00000508110.1:n.*204+259G=
ENST00000683735.1:c.*1924+259G=	ENSP00000508336.1:n.*1924+259G=
ENST00000683853.1:c.*590G=	ENSP00000506834.1:n.*590G=
ENST00000683860.1:c.*646+259G=	ENSP00000507179.1:n.*646+259G=
ENST00000684125.1:c.*186+259G=	ENSP00000507320.1:n.*186+259G=
ENST00000684203.1:n.3975+259G=
ENST00000684231.1:c.*936+259G=	ENSP00000507748.1:n.*936+259G=
ENST00000684263.1:c.*1150+259G=	ENSP00000508369.1:n.*1150+259G=
ENST00000684305.1:c.1974+259G=	ENSP00000506819.1:n.1974+259G=
ENST00000684602.1:c.*1192+259G=	ENSP00000507996.1:n.*1192+259G=
ENST00000684667.1:c.1857+259G=	ENSP00000507003.1:n.1857+259G=
ENST00000268097.10:c.1526+259G= MANE Select	ENSP00000268097.6:n.1526+259G=
ENST00000268097.9:c.1526+259G=	ENSP00000268097.5:n.1526+259G=
ENST00000379915.4:c.608+259G=	ENSP00000478716.1:n.608+259G=
ENST00000564677.5:n.318+259G=
ENST00000565873.1:n.437+259G=
ENST00000566304.5:c.1559+259G=	ENSP00000455114.1:n.1559+259G=
ENST00000567411.5:c.*1047+259G=	ENSP00000455545.1:n.*1047+259G=
NM_000520.4:c.1526+259G=	NP_000511.2:n.1526+259G=
NM_000520.5:c.1526+259G=	NP_000511.2:n.1526+259G=
NM_001318825.1:c.1559+259G=	NP_001305754.1:n.1559+259G=
NM_000520.6:c.1526+259G= MANE Select	NP_000511.2:n.1526+259G=
NM_001318825.2:c.1559+259G=	NP_001305754.1:n.1559+259G=