Canonical Allele Identifier: CA393062013

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72640471A>C (hg19) ; chr15:g.72348130A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72348130A>C , CM000677.2:g.72348130A>C	GRCh38
NC_000015.9:g.72640471A>C , CM000677.1:g.72640471A>C	GRCh37
NC_000015.8:g.70427525A>C	NCBI36
NG_009017.1:g.33050T>G
NG_009017.2:g.33050T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563908.2:n.3337T>G
ENST00000567027.6:c.991T>G	ENSP00000457521.2:p.Ser331Ala
ENST00000682061.1:c.*653T>G	ENSP00000508316.1:n.*653T>G
ENST00000682177.1:c.1034T>G	ENSP00000507409.1:n.1034T>G
ENST00000682461.1:c.1097T>G	ENSP00000507308.1:n.1097T>G
ENST00000682653.1:n.1022T>G
ENST00000682657.1:c.*401T>G	ENSP00000507753.1:n.*401T>G
ENST00000682721.1:c.*794T>G	ENSP00000507535.1:n.*794T>G
ENST00000682843.1:c.*889T>G	ENSP00000508173.1:n.*889T>G
ENST00000683003.1:c.*401T>G	ENSP00000507576.1:n.*401T>G
ENST00000683133.1:c.1175T>G	ENSP00000508108.1:n.1175T>G
ENST00000683228.1:n.1022T>G
ENST00000683243.1:c.*401T>G	ENSP00000507042.1:n.*401T>G
ENST00000683463.1:c.991T>G	ENSP00000507986.1:p.Ser331Ala
ENST00000683548.1:n.1022T>G
ENST00000683579.1:c.*889T>G	ENSP00000506867.1:n.*889T>G
ENST00000683587.1:n.1022T>G
ENST00000683681.1:c.991T>G	ENSP00000508110.1:p.Ser331Ala
ENST00000683735.1:c.*889T>G	ENSP00000508336.1:n.*889T>G
ENST00000683742.1:n.822T>G
ENST00000683853.1:c.991T>G	ENSP00000506834.1:p.Ser331Ala
ENST00000683860.1:c.991T>G	ENSP00000507179.1:p.Ser331Ala
ENST00000683884.1:c.991T>G	ENSP00000507004.1:p.Ser331Ala
ENST00000684041.1:c.991T>G	ENSP00000508382.1:p.Ser331Ala
ENST00000684125.1:c.991T>G	ENSP00000507320.1:p.Ser331Ala
ENST00000684203.1:n.2829T>G
ENST00000684231.1:c.*401T>G	ENSP00000507748.1:n.*401T>G
ENST00000684263.1:c.991T>G	ENSP00000508369.1:p.Ser331Ala
ENST00000684305.1:c.1439T>G	ENSP00000506819.1:n.1439T>G
ENST00000684415.1:c.991T>G	ENSP00000507227.1:p.Ser331Ala
ENST00000684520.1:c.991T>G	ENSP00000506826.1:p.Ser331Ala
ENST00000684602.1:c.*657T>G	ENSP00000507996.1:n.*657T>G
ENST00000684667.1:c.1322T>G	ENSP00000507003.1:n.1322T>G
ENST00000268097.10:c.991T>G MANE Select	ENSP00000268097.6:p.Ser331Ala
ENST00000268097.9:c.991T>G	ENSP00000268097.5:p.Ser331Ala
ENST00000379915.4:c.413-1805T>G	ENSP00000478716.1:n.413-1805T>G
ENST00000563762.5:c.743T>G	ENSP00000456346.1:n.743T>G
ENST00000566304.5:c.1024T>G	ENSP00000455114.1:p.Ser342Ala
ENST00000566672.5:c.*401T>G	ENSP00000457037.1:n.*401T>G
ENST00000567027.5:c.863T>G
ENST00000567159.5:c.991T>G	ENSP00000456489.1:p.Ser331Ala
ENST00000567411.5:c.*512T>G	ENSP00000455545.1:n.*512T>G
ENST00000568777.5:n.6395T>G
ENST00000569410.5:c.991T>G	ENSP00000457125.1:p.Ser331Ala
NM_000520.4:c.991T>G	NP_000511.2:p.Ser331Ala
NM_000520.5:c.991T>G	NP_000511.2:p.Ser331Ala
NM_001318825.1:c.1024T>G	NP_001305754.1:p.Ser342Ala
NR_134869.1:n.1492T>G
NM_000520.6:c.991T>G MANE Select	NP_000511.2:p.Ser331Ala
NM_001318825.2:c.1024T>G	NP_001305754.1:p.Ser342Ala
NR_134869.2:n.1033T>G
NR_134869.3:n.1033T>G