Canonical Allele Identifier: CA393066611

Gene: HEXA

Linked Data

• gnomAD v4: 15-72355568-C-T
• MyVariant Identifiers: chr15:g.72647909C>T (hg19) ; chr15:g.72355568C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72355568C>T , CM000677.2:g.72355568C>T	GRCh38
NC_000015.9:g.72647909C>T , CM000677.1:g.72647909C>T	GRCh37
NC_000015.8:g.70434963C>T	NCBI36
NG_009017.1:g.25612G>A
NG_009017.2:g.25612G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563908.2:n.416G>A
ENST00000567027.6:c.403G>A	ENSP00000457521.2:p.Ala135Thr
ENST00000568260.2:c.470G>A	ENSP00000458128.2:n.470G>A
ENST00000682061.1:c.*65G>A	ENSP00000508316.1:n.*65G>A
ENST00000682177.1:c.403G>A	ENSP00000507409.1:p.Ala135Thr
ENST00000682461.1:c.667G>A	ENSP00000507308.1:n.667G>A
ENST00000682653.1:n.434G>A
ENST00000682657.1:c.254-4334G>A	ENSP00000507753.1:n.254-4334G>A
ENST00000682721.1:c.*206G>A	ENSP00000507535.1:n.*206G>A
ENST00000682843.1:c.*301G>A	ENSP00000508173.1:n.*301G>A
ENST00000683003.1:c.403G>A	ENSP00000507576.1:p.Ala135Thr
ENST00000683133.1:c.587G>A	ENSP00000508108.1:n.587G>A
ENST00000683228.1:n.434G>A
ENST00000683243.1:c.403G>A	ENSP00000507042.1:p.Ala135Thr
ENST00000683463.1:c.403G>A	ENSP00000507986.1:p.Ala135Thr
ENST00000683548.1:n.434G>A
ENST00000683579.1:c.*301G>A	ENSP00000506867.1:n.*301G>A
ENST00000683587.1:n.434G>A
ENST00000683681.1:c.403G>A	ENSP00000508110.1:p.Ala135Thr
ENST00000683735.1:c.*301G>A	ENSP00000508336.1:n.*301G>A
ENST00000683853.1:c.403G>A	ENSP00000506834.1:p.Ala135Thr
ENST00000683860.1:c.403G>A	ENSP00000507179.1:p.Ala135Thr
ENST00000683884.1:c.403G>A	ENSP00000507004.1:p.Ala135Thr
ENST00000684041.1:c.403G>A	ENSP00000508382.1:p.Ala135Thr
ENST00000684125.1:c.403G>A	ENSP00000507320.1:p.Ala135Thr
ENST00000684203.1:n.420G>A
ENST00000684231.1:c.403G>A	ENSP00000507748.1:p.Ala135Thr
ENST00000684263.1:c.403G>A	ENSP00000508369.1:p.Ala135Thr
ENST00000684305.1:c.851G>A	ENSP00000506819.1:n.851G>A
ENST00000684415.1:c.403G>A	ENSP00000507227.1:p.Ala135Thr
ENST00000684520.1:c.403G>A	ENSP00000506826.1:p.Ala135Thr
ENST00000684602.1:c.*227G>A	ENSP00000507996.1:n.*227G>A
ENST00000684667.1:c.734G>A	ENSP00000507003.1:n.734G>A
ENST00000268097.10:c.403G>A MANE Select	ENSP00000268097.6:p.Ala135Thr
ENST00000268097.9:c.403G>A	ENSP00000268097.5:p.Ala135Thr
ENST00000379915.4:c.403G>A	ENSP00000478716.1:p.Ala135Thr
ENST00000563762.5:c.494G>A	ENSP00000456346.1:n.494G>A
ENST00000563908.1:n.400G>A
ENST00000566304.5:c.436G>A	ENSP00000455114.1:p.Ala146Thr
ENST00000566672.5:c.403G>A	ENSP00000457037.1:p.Ala135Thr
ENST00000567027.5:c.275G>A
ENST00000567159.5:c.403G>A	ENSP00000456489.1:p.Ala135Thr
ENST00000567411.5:c.403G>A	ENSP00000455545.1:p.Ala135Thr
ENST00000568260.1:c.451G>A
ENST00000568777.5:n.3986G>A
ENST00000569410.5:c.403G>A	ENSP00000457125.1:p.Ala135Thr
ENST00000569509.5:n.408G>A
NM_000520.4:c.403G>A	NP_000511.2:p.Ala135Thr
NM_000520.5:c.403G>A	NP_000511.2:p.Ala135Thr
NM_001318825.1:c.436G>A	NP_001305754.1:p.Ala146Thr
NR_134869.1:n.904G>A
NM_000520.6:c.403G>A MANE Select	NP_000511.2:p.Ala135Thr
NM_001318825.2:c.436G>A	NP_001305754.1:p.Ala146Thr
NR_134869.2:n.445G>A
NR_134869.3:n.445G>A