Canonical Allele Identifier: CA2186743162
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345277T= , CM000677.2:g.72345277T= GRCh38
NC_000015.9:g.72637618T= , CM000677.1:g.72637618T= GRCh37
NC_000015.8:g.70424672T= NCBI36
NG_009017.1:g.35903A=
NG_009017.2:g.35903A=

Transcript Alleles

HGVS Amino-acid change
ENST00000567027.6:c.*355A= ENSP00000457521.2:n.*355A=
ENST00000682061.1:c.*2041A= ENSP00000508316.1:n.*2041A=
ENST00000682064.1:n.1753+169A=
ENST00000682177.1:c.1738A= ENSP00000507409.1:n.1738A=
ENST00000682235.1:n.1549+169A=
ENST00000682461.1:c.1632+169A= ENSP00000507308.1:n.1632+169A=
ENST00000682653.1:n.2699A=
ENST00000682657.1:c.*1532A= ENSP00000507753.1:n.*1532A=
ENST00000682721.1:c.*1329+169A= ENSP00000507535.1:n.*1329+169A=
ENST00000682843.1:c.*1167+169A= ENSP00000508173.1:n.*1167+169A=
ENST00000683133.1:c.1710+169A= ENSP00000508108.1:n.1710+169A=
ENST00000683243.1:c.*679+169A= ENSP00000507042.1:n.*679+169A=
ENST00000683463.1:c.*1015+169A= ENSP00000507986.1:n.*1015+169A=
ENST00000683548.1:n.1984+169A=
ENST00000683579.1:c.*1424+169A= ENSP00000506867.1:n.*1424+169A=
ENST00000683587.1:n.2057+169A=
ENST00000683681.1:c.*204+169A= ENSP00000508110.1:n.*204+169A=
ENST00000683735.1:c.*1924+169A= ENSP00000508336.1:n.*1924+169A=
ENST00000683853.1:c.*500A= ENSP00000506834.1:n.*500A=
ENST00000683860.1:c.*646+169A= ENSP00000507179.1:n.*646+169A=
ENST00000683884.1:c.*1022A= ENSP00000507004.1:n.*1022A=
ENST00000684125.1:c.*186+169A= ENSP00000507320.1:n.*186+169A=
ENST00000684203.1:n.3975+169A=
ENST00000684231.1:c.*936+169A= ENSP00000507748.1:n.*936+169A=
ENST00000684263.1:c.*1150+169A= ENSP00000508369.1:n.*1150+169A=
ENST00000684305.1:c.1974+169A= ENSP00000506819.1:n.1974+169A=
ENST00000684415.1:c.*1246A= ENSP00000507227.1:n.*1246A=
ENST00000684520.1:c.*954A= ENSP00000506826.1:n.*954A=
ENST00000684602.1:c.*1192+169A= ENSP00000507996.1:n.*1192+169A=
ENST00000684667.1:c.1857+169A= ENSP00000507003.1:n.1857+169A=
ENST00000268097.10:c.1526+169A= MANE Select ENSP00000268097.6:n.1526+169A=
ENST00000268097.9:c.1526+169A= ENSP00000268097.5:n.1526+169A=
ENST00000379915.4:c.608+169A= ENSP00000478716.1:n.608+169A=
ENST00000564677.5:n.318+169A=
ENST00000565873.1:n.437+169A=
ENST00000566304.5:c.1559+169A= ENSP00000455114.1:n.1559+169A=
ENST00000567027.5:c.1310A=
ENST00000567411.5:c.*1047+169A= ENSP00000455545.1:n.*1047+169A=
ENST00000569116.1:n.402A=
NM_000520.4:c.1526+169A= NP_000511.2:n.1526+169A=
NM_000520.5:c.1526+169A= NP_000511.2:n.1526+169A=
NM_001318825.1:c.1559+169A= NP_001305754.1:n.1559+169A=
NR_134869.1:n.1939A=
NM_000520.6:c.1526+169A= MANE Select NP_000511.2:n.1526+169A=
NM_001318825.2:c.1559+169A= NP_001305754.1:n.1559+169A=
NR_134869.2:n.1480A=
NR_134869.3:n.1480A=