Canonical Allele Identifier: CA2186743265
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345476C= , CM000677.2:g.72345476C= GRCh38
NC_000015.9:g.72637817C= , CM000677.1:g.72637817C= GRCh37
NC_000015.8:g.70424871C= NCBI36
NG_009017.1:g.35704G=
NG_009017.2:g.35704G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*156G= ENSP00000457521.2:n.*156G=
ENST00000682061.1:c.*1842G= ENSP00000508316.1:n.*1842G=
ENST00000682064.1:n.1723G=
ENST00000682177.1:c.1539G= ENSP00000507409.1:n.1539G=
ENST00000682235.1:n.1519G=
ENST00000682461.1:c.1602G= ENSP00000507308.1:n.1602G=
ENST00000682653.1:n.2500G=
ENST00000682657.1:c.*1333G= ENSP00000507753.1:n.*1333G=
ENST00000682721.1:c.*1299G= ENSP00000507535.1:n.*1299G=
ENST00000682843.1:c.*1137G= ENSP00000508173.1:n.*1137G=
ENST00000683003.1:c.*1333G= ENSP00000507576.1:n.*1333G=
ENST00000683133.1:c.1680G= ENSP00000508108.1:n.1680G=
ENST00000683243.1:c.*649G= ENSP00000507042.1:n.*649G=
ENST00000683463.1:c.*985G= ENSP00000507986.1:n.*985G=
ENST00000683548.1:n.1954G=
ENST00000683579.1:c.*1394G= ENSP00000506867.1:n.*1394G=
ENST00000683587.1:n.2027G=
ENST00000683681.1:c.*174G= ENSP00000508110.1:n.*174G=
ENST00000683735.1:c.*1894G= ENSP00000508336.1:n.*1894G=
ENST00000683853.1:c.*301G= ENSP00000506834.1:n.*301G=
ENST00000683860.1:c.*616G= ENSP00000507179.1:n.*616G=
ENST00000683884.1:c.*823G= ENSP00000507004.1:n.*823G=
ENST00000684041.1:c.*629G= ENSP00000508382.1:n.*629G=
ENST00000684125.1:c.*156G= ENSP00000507320.1:n.*156G=
ENST00000684203.1:n.3945G=
ENST00000684231.1:c.*906G= ENSP00000507748.1:n.*906G=
ENST00000684263.1:c.*1120G= ENSP00000508369.1:n.*1120G=
ENST00000684305.1:c.1944G= ENSP00000506819.1:n.1944G=
ENST00000684415.1:c.*1047G= ENSP00000507227.1:n.*1047G=
ENST00000684520.1:c.*755G= ENSP00000506826.1:n.*755G=
ENST00000684602.1:c.*1162G= ENSP00000507996.1:n.*1162G=
ENST00000684667.1:c.1827G= ENSP00000507003.1:n.1827G=
ENST00000268097.10:c.1496G= MANE Select ENSP00000268097.6:p.Arg499=
ENST00000268097.9:c.1496G= ENSP00000268097.5:p.Arg499=
ENST00000379915.4:c.578G= ENSP00000478716.1:p.Arg193=
ENST00000564677.5:n.288G=
ENST00000565873.1:n.407G=
ENST00000566304.5:c.1529G= ENSP00000455114.1:p.Arg510=
ENST00000567027.5:c.1111G=
ENST00000567159.5:c.1496G= ENSP00000456489.1:p.Arg499=
ENST00000567411.5:c.*1017G= ENSP00000455545.1:n.*1017G=
ENST00000568777.5:n.6716G=
ENST00000569116.1:n.203G=
NM_000520.4:c.1496G= NP_000511.2:p.Arg499=
NM_000520.5:c.1496G= NP_000511.2:p.Arg499=
NM_001318825.1:c.1529G= NP_001305754.1:p.Arg510=
NR_134869.1:n.1740G=
NM_000520.6:c.1496G= MANE Select NP_000511.2:p.Arg499=
NM_001318825.2:c.1529G= NP_001305754.1:p.Arg510=
NR_134869.2:n.1281G=
NR_134869.3:n.1281G=