Canonical Allele Identifier: CA2186743274
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345496G= , CM000677.2:g.72345496G= GRCh38
NC_000015.9:g.72637837G= , CM000677.1:g.72637837G= GRCh37
NC_000015.8:g.70424891G= NCBI36
NG_009017.1:g.35684C=
NG_009017.2:g.35684C=

Transcript Alleles

HGVS Amino-acid change
ENST00000567027.6:c.*136C= ENSP00000457521.2:n.*136C=
ENST00000682061.1:c.*1822C= ENSP00000508316.1:n.*1822C=
ENST00000682064.1:n.1703C=
ENST00000682177.1:c.1519C= ENSP00000507409.1:n.1519C=
ENST00000682235.1:n.1499C=
ENST00000682461.1:c.1582C= ENSP00000507308.1:n.1582C=
ENST00000682653.1:n.2480C=
ENST00000682657.1:c.*1313C= ENSP00000507753.1:n.*1313C=
ENST00000682721.1:c.*1279C= ENSP00000507535.1:n.*1279C=
ENST00000682843.1:c.*1117C= ENSP00000508173.1:n.*1117C=
ENST00000683003.1:c.*1313C= ENSP00000507576.1:n.*1313C=
ENST00000683133.1:c.1660C= ENSP00000508108.1:n.1660C=
ENST00000683243.1:c.*629C= ENSP00000507042.1:n.*629C=
ENST00000683463.1:c.*965C= ENSP00000507986.1:n.*965C=
ENST00000683548.1:n.1934C=
ENST00000683579.1:c.*1374C= ENSP00000506867.1:n.*1374C=
ENST00000683587.1:n.2007C=
ENST00000683681.1:c.*154C= ENSP00000508110.1:n.*154C=
ENST00000683735.1:c.*1874C= ENSP00000508336.1:n.*1874C=
ENST00000683853.1:c.*281C= ENSP00000506834.1:n.*281C=
ENST00000683860.1:c.*596C= ENSP00000507179.1:n.*596C=
ENST00000683884.1:c.*803C= ENSP00000507004.1:n.*803C=
ENST00000684041.1:c.*609C= ENSP00000508382.1:n.*609C=
ENST00000684125.1:c.*136C= ENSP00000507320.1:n.*136C=
ENST00000684203.1:n.3925C=
ENST00000684231.1:c.*886C= ENSP00000507748.1:n.*886C=
ENST00000684263.1:c.*1100C= ENSP00000508369.1:n.*1100C=
ENST00000684305.1:c.1924C= ENSP00000506819.1:n.1924C=
ENST00000684415.1:c.*1027C= ENSP00000507227.1:n.*1027C=
ENST00000684520.1:c.*735C= ENSP00000506826.1:n.*735C=
ENST00000684602.1:c.*1142C= ENSP00000507996.1:n.*1142C=
ENST00000684667.1:c.1807C= ENSP00000507003.1:n.1807C=
ENST00000268097.10:c.1476C= MANE Select ENSP00000268097.6:p.Asp492=
ENST00000268097.9:c.1476C= ENSP00000268097.5:p.Asp492=
ENST00000379915.4:c.558C= ENSP00000478716.1:p.Asp186=
ENST00000564677.5:n.268C=
ENST00000565873.1:n.387C=
ENST00000566304.5:c.1509C= ENSP00000455114.1:p.Asp503=
ENST00000567027.5:c.1091C=
ENST00000567159.5:c.1476C= ENSP00000456489.1:p.Asp492=
ENST00000567411.5:c.*997C= ENSP00000455545.1:n.*997C=
ENST00000568777.5:n.6696C=
ENST00000569116.1:n.183C=
NM_000520.4:c.1476C= NP_000511.2:p.Asp492=
NM_000520.5:c.1476C= NP_000511.2:p.Asp492=
NM_001318825.1:c.1509C= NP_001305754.1:p.Asp503=
NR_134869.1:n.1720C=
NM_000520.6:c.1476C= MANE Select NP_000511.2:p.Asp492=
NM_001318825.2:c.1509C= NP_001305754.1:p.Asp503=
NR_134869.2:n.1261C=
NR_134869.3:n.1261C=