Canonical Allele Identifier: CA2186743275
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345497T= , CM000677.2:g.72345497T= GRCh38
NC_000015.9:g.72637838T= , CM000677.1:g.72637838T= GRCh37
NC_000015.8:g.70424892T= NCBI36
NG_009017.1:g.35683A=
NG_009017.2:g.35683A=

Transcript Alleles

HGVS Amino-acid change
ENST00000567027.6:c.*135A= ENSP00000457521.2:n.*135A=
ENST00000682061.1:c.*1821A= ENSP00000508316.1:n.*1821A=
ENST00000682064.1:n.1702A=
ENST00000682177.1:c.1518A= ENSP00000507409.1:n.1518A=
ENST00000682235.1:n.1498A=
ENST00000682461.1:c.1581A= ENSP00000507308.1:n.1581A=
ENST00000682653.1:n.2479A=
ENST00000682657.1:c.*1312A= ENSP00000507753.1:n.*1312A=
ENST00000682721.1:c.*1278A= ENSP00000507535.1:n.*1278A=
ENST00000682843.1:c.*1116A= ENSP00000508173.1:n.*1116A=
ENST00000683003.1:c.*1312A= ENSP00000507576.1:n.*1312A=
ENST00000683133.1:c.1659A= ENSP00000508108.1:n.1659A=
ENST00000683243.1:c.*628A= ENSP00000507042.1:n.*628A=
ENST00000683463.1:c.*964A= ENSP00000507986.1:n.*964A=
ENST00000683548.1:n.1933A=
ENST00000683579.1:c.*1373A= ENSP00000506867.1:n.*1373A=
ENST00000683587.1:n.2006A=
ENST00000683681.1:c.*153A= ENSP00000508110.1:n.*153A=
ENST00000683735.1:c.*1873A= ENSP00000508336.1:n.*1873A=
ENST00000683853.1:c.*280A= ENSP00000506834.1:n.*280A=
ENST00000683860.1:c.*595A= ENSP00000507179.1:n.*595A=
ENST00000683884.1:c.*802A= ENSP00000507004.1:n.*802A=
ENST00000684041.1:c.*608A= ENSP00000508382.1:n.*608A=
ENST00000684125.1:c.*135A= ENSP00000507320.1:n.*135A=
ENST00000684203.1:n.3924A=
ENST00000684231.1:c.*885A= ENSP00000507748.1:n.*885A=
ENST00000684263.1:c.*1099A= ENSP00000508369.1:n.*1099A=
ENST00000684305.1:c.1923A= ENSP00000506819.1:n.1923A=
ENST00000684415.1:c.*1026A= ENSP00000507227.1:n.*1026A=
ENST00000684520.1:c.*734A= ENSP00000506826.1:n.*734A=
ENST00000684602.1:c.*1141A= ENSP00000507996.1:n.*1141A=
ENST00000684667.1:c.1806A= ENSP00000507003.1:n.1806A=
ENST00000268097.10:c.1475A= MANE Select ENSP00000268097.6:p.Asp492=
ENST00000268097.9:c.1475A= ENSP00000268097.5:p.Asp492=
ENST00000379915.4:c.557A= ENSP00000478716.1:p.Asp186=
ENST00000564677.5:n.267A=
ENST00000565873.1:n.386A=
ENST00000566304.5:c.1508A= ENSP00000455114.1:p.Asp503=
ENST00000567027.5:c.1090A=
ENST00000567159.5:c.1475A= ENSP00000456489.1:p.Asp492=
ENST00000567411.5:c.*996A= ENSP00000455545.1:n.*996A=
ENST00000568777.5:n.6695A=
ENST00000569116.1:n.182A=
NM_000520.4:c.1475A= NP_000511.2:p.Asp492=
NM_000520.5:c.1475A= NP_000511.2:p.Asp492=
NM_001318825.1:c.1508A= NP_001305754.1:p.Asp503=
NR_134869.1:n.1719A=
NM_000520.6:c.1475A= MANE Select NP_000511.2:p.Asp492=
NM_001318825.2:c.1508A= NP_001305754.1:p.Asp503=
NR_134869.2:n.1260A=
NR_134869.3:n.1260A=