Canonical Allele Identifier: CA491119539

Gene: HEXA

Linked Data

• ClinVar Variation Id: 3003498
• ClinVar RCV Id: RCV003868113
• MyVariant Identifiers: chr15:g.72641467T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72349126T>C , CM000677.2:g.72349126T>C	GRCh38
NC_000015.9:g.72641467T>C , CM000677.1:g.72641467T>C	GRCh37
NC_000015.8:g.70428521T>C	NCBI36
NG_009017.1:g.32054A>G
NG_009017.2:g.32054A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563908.2:n.3285A>G
ENST00000567027.6:c.939A>G	ENSP00000457521.2:p.Pro313=
ENST00000682061.1:c.*601A>G	ENSP00000508316.1:n.*601A>G
ENST00000682177.1:c.982A>G	ENSP00000507409.1:n.982A>G
ENST00000682461.1:c.1045A>G	ENSP00000507308.1:n.1045A>G
ENST00000682653.1:n.970A>G
ENST00000682657.1:c.*349A>G	ENSP00000507753.1:n.*349A>G
ENST00000682721.1:c.*742A>G	ENSP00000507535.1:n.*742A>G
ENST00000682843.1:c.*837A>G	ENSP00000508173.1:n.*837A>G
ENST00000683003.1:c.*349A>G	ENSP00000507576.1:n.*349A>G
ENST00000683133.1:c.1123A>G	ENSP00000508108.1:n.1123A>G
ENST00000683228.1:n.970A>G
ENST00000683243.1:c.*349A>G	ENSP00000507042.1:n.*349A>G
ENST00000683463.1:c.939A>G	ENSP00000507986.1:p.Pro313=
ENST00000683548.1:n.970A>G
ENST00000683579.1:c.*837A>G	ENSP00000506867.1:n.*837A>G
ENST00000683587.1:n.970A>G
ENST00000683681.1:c.939A>G	ENSP00000508110.1:p.Pro313=
ENST00000683735.1:c.*837A>G	ENSP00000508336.1:n.*837A>G
ENST00000683742.1:n.770A>G
ENST00000683853.1:c.939A>G	ENSP00000506834.1:p.Pro313=
ENST00000683860.1:c.939A>G	ENSP00000507179.1:p.Pro313=
ENST00000683884.1:c.939A>G	ENSP00000507004.1:p.Pro313=
ENST00000684041.1:c.939A>G	ENSP00000508382.1:p.Pro313=
ENST00000684125.1:c.939A>G	ENSP00000507320.1:p.Pro313=
ENST00000684203.1:n.2777A>G
ENST00000684231.1:c.*349A>G	ENSP00000507748.1:n.*349A>G
ENST00000684263.1:c.939A>G	ENSP00000508369.1:p.Pro313=
ENST00000684305.1:c.1387A>G	ENSP00000506819.1:n.1387A>G
ENST00000684415.1:c.939A>G	ENSP00000507227.1:p.Pro313=
ENST00000684520.1:c.939A>G	ENSP00000506826.1:p.Pro313=
ENST00000684602.1:c.*605A>G	ENSP00000507996.1:n.*605A>G
ENST00000684667.1:c.1270A>G	ENSP00000507003.1:n.1270A>G
ENST00000268097.10:c.939A>G MANE Select	ENSP00000268097.6:p.Pro313=
ENST00000268097.9:c.939A>G	ENSP00000268097.5:p.Pro313=
ENST00000379915.4:c.413-2801A>G	ENSP00000478716.1:n.413-2801A>G
ENST00000563762.5:c.739-992A>G	ENSP00000456346.1:n.739-992A>G
ENST00000566304.5:c.972A>G	ENSP00000455114.1:p.Pro324=
ENST00000566672.5:c.*349A>G	ENSP00000457037.1:n.*349A>G
ENST00000567027.5:c.811A>G
ENST00000567159.5:c.939A>G	ENSP00000456489.1:p.Pro313=
ENST00000567411.5:c.*460A>G	ENSP00000455545.1:n.*460A>G
ENST00000568777.5:n.6343A>G
ENST00000569410.5:c.939A>G	ENSP00000457125.1:p.Pro313=
NM_000520.4:c.939A>G	NP_000511.2:p.Pro313=
NM_000520.5:c.939A>G	NP_000511.2:p.Pro313=
NM_001318825.1:c.972A>G	NP_001305754.1:p.Pro324=
NR_134869.1:n.1440A>G
NM_000520.6:c.939A>G MANE Select	NP_000511.2:p.Pro313=
NM_001318825.2:c.972A>G	NP_001305754.1:p.Pro324=
NR_134869.2:n.981A>G
NR_134869.3:n.981A>G