Canonical Allele Identifier: CA393061631

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72640038T>A (hg19) ; chr15:g.72347697T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72347697T>A , CM000677.2:g.72347697T>A	GRCh38
NC_000015.9:g.72640038T>A , CM000677.1:g.72640038T>A	GRCh37
NC_000015.8:g.70427092T>A	NCBI36
NG_009017.1:g.33483A>T
NG_009017.2:g.33483A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000567027.6:c.1073+351A>T	ENSP00000457521.2:n.1073+351A>T
ENST00000682061.1:c.*797A>T	ENSP00000508316.1:n.*797A>T
ENST00000682177.1:c.1178A>T	ENSP00000507409.1:n.1178A>T
ENST00000682461.1:c.1241A>T	ENSP00000507308.1:n.1241A>T
ENST00000682653.1:n.1455A>T
ENST00000682657.1:c.*483+351A>T	ENSP00000507753.1:n.*483+351A>T
ENST00000682721.1:c.*938A>T	ENSP00000507535.1:n.*938A>T
ENST00000682843.1:c.*971+351A>T	ENSP00000508173.1:n.*971+351A>T
ENST00000683003.1:c.*483+351A>T	ENSP00000507576.1:n.*483+351A>T
ENST00000683133.1:c.1319A>T	ENSP00000508108.1:n.1319A>T
ENST00000683228.1:n.1166A>T
ENST00000683243.1:c.*483+351A>T	ENSP00000507042.1:n.*483+351A>T
ENST00000683463.1:c.1073+351A>T	ENSP00000507986.1:n.1073+351A>T
ENST00000683548.1:n.1104+351A>T
ENST00000683579.1:c.*1033A>T	ENSP00000506867.1:n.*1033A>T
ENST00000683587.1:n.1166A>T
ENST00000683681.1:c.1135A>T	ENSP00000508110.1:p.Asn379Tyr
ENST00000683735.1:c.*1033A>T	ENSP00000508336.1:n.*1033A>T
ENST00000683742.1:n.966A>T
ENST00000683853.1:c.1073+351A>T	ENSP00000506834.1:n.1073+351A>T
ENST00000683860.1:c.1135A>T	ENSP00000507179.1:p.Asn379Tyr
ENST00000683884.1:c.1135A>T	ENSP00000507004.1:p.Asn379Tyr
ENST00000684041.1:c.1135A>T	ENSP00000508382.1:p.Asn379Tyr
ENST00000684125.1:c.1073+351A>T	ENSP00000507320.1:n.1073+351A>T
ENST00000684203.1:n.2911+351A>T
ENST00000684231.1:c.*545A>T	ENSP00000507748.1:n.*545A>T
ENST00000684263.1:c.*75A>T	ENSP00000508369.1:n.*75A>T
ENST00000684305.1:c.1583A>T	ENSP00000506819.1:n.1583A>T
ENST00000684415.1:c.*13+334A>T	ENSP00000507227.1:n.*13+334A>T
ENST00000684520.1:c.1135A>T	ENSP00000506826.1:p.Asn379Tyr
ENST00000684602.1:c.*801A>T	ENSP00000507996.1:n.*801A>T
ENST00000684667.1:c.1466A>T	ENSP00000507003.1:n.1466A>T
ENST00000268097.10:c.1135A>T MANE Select	ENSP00000268097.6:p.Asn379Tyr
ENST00000268097.9:c.1135A>T	ENSP00000268097.5:p.Asn379Tyr
ENST00000379915.4:c.413-1372A>T	ENSP00000478716.1:n.413-1372A>T
ENST00000563762.5:c.825+351A>T	ENSP00000456346.1:n.825+351A>T
ENST00000566304.5:c.1168A>T	ENSP00000455114.1:p.Asn390Tyr
ENST00000566672.5:c.*545A>T	ENSP00000457037.1:n.*545A>T
ENST00000567027.5:c.945+351A>T
ENST00000567159.5:c.1135A>T	ENSP00000456489.1:p.Asn379Tyr
ENST00000567411.5:c.*656A>T	ENSP00000455545.1:n.*656A>T
ENST00000568777.5:n.6539A>T
ENST00000569410.5:c.1073+351A>T	ENSP00000457125.1:n.1073+351A>T
NM_000520.4:c.1135A>T	NP_000511.2:p.Asn379Tyr
NM_000520.5:c.1135A>T	NP_000511.2:p.Asn379Tyr
NM_001318825.1:c.1168A>T	NP_001305754.1:p.Asn390Tyr
NR_134869.1:n.1574+351A>T
NM_000520.6:c.1135A>T MANE Select	NP_000511.2:p.Asn379Tyr
NM_001318825.2:c.1168A>T	NP_001305754.1:p.Asn390Tyr
NR_134869.2:n.1115+351A>T
NR_134869.3:n.1115+351A>T