Canonical Allele Identifier: CA393061897

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72640422T>A (hg19) ; chr15:g.72348081T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72348081T>A , CM000677.2:g.72348081T>A	GRCh38
NC_000015.9:g.72640422T>A , CM000677.1:g.72640422T>A	GRCh37
NC_000015.8:g.70427476T>A	NCBI36
NG_009017.1:g.33099A>T
NG_009017.2:g.33099A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000563908.2:n.3386A>T
ENST00000567027.6:c.1040A>T	ENSP00000457521.2:p.Asp347Val
ENST00000682061.1:c.*702A>T	ENSP00000508316.1:n.*702A>T
ENST00000682177.1:c.1083A>T	ENSP00000507409.1:n.1083A>T
ENST00000682461.1:c.1146A>T	ENSP00000507308.1:n.1146A>T
ENST00000682653.1:n.1071A>T
ENST00000682657.1:c.*450A>T	ENSP00000507753.1:n.*450A>T
ENST00000682721.1:c.*843A>T	ENSP00000507535.1:n.*843A>T
ENST00000682843.1:c.*938A>T	ENSP00000508173.1:n.*938A>T
ENST00000683003.1:c.*450A>T	ENSP00000507576.1:n.*450A>T
ENST00000683133.1:c.1224A>T	ENSP00000508108.1:n.1224A>T
ENST00000683228.1:n.1071A>T
ENST00000683243.1:c.*450A>T	ENSP00000507042.1:n.*450A>T
ENST00000683463.1:c.1040A>T	ENSP00000507986.1:p.Asp347Val
ENST00000683548.1:n.1071A>T
ENST00000683579.1:c.*938A>T	ENSP00000506867.1:n.*938A>T
ENST00000683587.1:n.1071A>T
ENST00000683681.1:c.1040A>T	ENSP00000508110.1:p.Asp347Val
ENST00000683735.1:c.*938A>T	ENSP00000508336.1:n.*938A>T
ENST00000683742.1:n.871A>T
ENST00000683853.1:c.1040A>T	ENSP00000506834.1:p.Asp347Val
ENST00000683860.1:c.1040A>T	ENSP00000507179.1:p.Asp347Val
ENST00000683884.1:c.1040A>T	ENSP00000507004.1:p.Asp347Val
ENST00000684041.1:c.1040A>T	ENSP00000508382.1:p.Asp347Val
ENST00000684125.1:c.1040A>T	ENSP00000507320.1:p.Asp347Val
ENST00000684203.1:n.2878A>T
ENST00000684231.1:c.*450A>T	ENSP00000507748.1:n.*450A>T
ENST00000684263.1:c.1040A>T	ENSP00000508369.1:p.Asp347Val
ENST00000684305.1:c.1488A>T	ENSP00000506819.1:n.1488A>T
ENST00000684415.1:c.1040A>T	ENSP00000507227.1:p.Asp347Val
ENST00000684520.1:c.1040A>T	ENSP00000506826.1:p.Asp347Val
ENST00000684602.1:c.*706A>T	ENSP00000507996.1:n.*706A>T
ENST00000684667.1:c.1371A>T	ENSP00000507003.1:n.1371A>T
ENST00000268097.10:c.1040A>T MANE Select	ENSP00000268097.6:p.Asp347Val
ENST00000268097.9:c.1040A>T	ENSP00000268097.5:p.Asp347Val
ENST00000379915.4:c.413-1756A>T	ENSP00000478716.1:n.413-1756A>T
ENST00000563762.5:c.792A>T	ENSP00000456346.1:n.792A>T
ENST00000566304.5:c.1073A>T	ENSP00000455114.1:p.Asp358Val
ENST00000566672.5:c.*450A>T	ENSP00000457037.1:n.*450A>T
ENST00000567027.5:c.912A>T
ENST00000567159.5:c.1040A>T	ENSP00000456489.1:p.Asp347Val
ENST00000567411.5:c.*561A>T	ENSP00000455545.1:n.*561A>T
ENST00000568777.5:n.6444A>T
ENST00000569410.5:c.1040A>T	ENSP00000457125.1:p.Asp347Val
NM_000520.4:c.1040A>T	NP_000511.2:p.Asp347Val
NM_000520.5:c.1040A>T	NP_000511.2:p.Asp347Val
NM_001318825.1:c.1073A>T	NP_001305754.1:p.Asp358Val
NR_134869.1:n.1541A>T
NM_000520.6:c.1040A>T MANE Select	NP_000511.2:p.Asp347Val
NM_001318825.2:c.1073A>T	NP_001305754.1:p.Asp358Val
NR_134869.2:n.1082A>T
NR_134869.3:n.1082A>T