Canonical Allele Identifier: CA2186743179
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345318G= , CM000677.2:g.72345318G= GRCh38
NC_000015.9:g.72637659G= , CM000677.1:g.72637659G= GRCh37
NC_000015.8:g.70424713G= NCBI36
NG_009017.1:g.35862C=
NG_009017.2:g.35862C=

Transcript Alleles

HGVS Amino-acid change
ENST00000567027.6:c.*314C= ENSP00000457521.2:n.*314C=
ENST00000682061.1:c.*2000C= ENSP00000508316.1:n.*2000C=
ENST00000682064.1:n.1753+128C=
ENST00000682177.1:c.1697C= ENSP00000507409.1:n.1697C=
ENST00000682235.1:n.1549+128C=
ENST00000682461.1:c.1632+128C= ENSP00000507308.1:n.1632+128C=
ENST00000682653.1:n.2658C=
ENST00000682657.1:c.*1491C= ENSP00000507753.1:n.*1491C=
ENST00000682721.1:c.*1329+128C= ENSP00000507535.1:n.*1329+128C=
ENST00000682843.1:c.*1167+128C= ENSP00000508173.1:n.*1167+128C=
ENST00000683133.1:c.1710+128C= ENSP00000508108.1:n.1710+128C=
ENST00000683243.1:c.*679+128C= ENSP00000507042.1:n.*679+128C=
ENST00000683463.1:c.*1015+128C= ENSP00000507986.1:n.*1015+128C=
ENST00000683548.1:n.1984+128C=
ENST00000683579.1:c.*1424+128C= ENSP00000506867.1:n.*1424+128C=
ENST00000683587.1:n.2057+128C=
ENST00000683681.1:c.*204+128C= ENSP00000508110.1:n.*204+128C=
ENST00000683735.1:c.*1924+128C= ENSP00000508336.1:n.*1924+128C=
ENST00000683853.1:c.*459C= ENSP00000506834.1:n.*459C=
ENST00000683860.1:c.*646+128C= ENSP00000507179.1:n.*646+128C=
ENST00000683884.1:c.*981C= ENSP00000507004.1:n.*981C=
ENST00000684125.1:c.*186+128C= ENSP00000507320.1:n.*186+128C=
ENST00000684203.1:n.3975+128C=
ENST00000684231.1:c.*936+128C= ENSP00000507748.1:n.*936+128C=
ENST00000684263.1:c.*1150+128C= ENSP00000508369.1:n.*1150+128C=
ENST00000684305.1:c.1974+128C= ENSP00000506819.1:n.1974+128C=
ENST00000684415.1:c.*1205C= ENSP00000507227.1:n.*1205C=
ENST00000684520.1:c.*913C= ENSP00000506826.1:n.*913C=
ENST00000684602.1:c.*1192+128C= ENSP00000507996.1:n.*1192+128C=
ENST00000684667.1:c.1857+128C= ENSP00000507003.1:n.1857+128C=
ENST00000268097.10:c.1526+128C= MANE Select ENSP00000268097.6:n.1526+128C=
ENST00000268097.9:c.1526+128C= ENSP00000268097.5:n.1526+128C=
ENST00000379915.4:c.608+128C= ENSP00000478716.1:n.608+128C=
ENST00000564677.5:n.318+128C=
ENST00000565873.1:n.437+128C=
ENST00000566304.5:c.1559+128C= ENSP00000455114.1:n.1559+128C=
ENST00000567027.5:c.1269C=
ENST00000567411.5:c.*1047+128C= ENSP00000455545.1:n.*1047+128C=
ENST00000568777.5:n.6874C=
ENST00000569116.1:n.361C=
NM_000520.4:c.1526+128C= NP_000511.2:n.1526+128C=
NM_000520.5:c.1526+128C= NP_000511.2:n.1526+128C=
NM_001318825.1:c.1559+128C= NP_001305754.1:n.1559+128C=
NR_134869.1:n.1898C=
NM_000520.6:c.1526+128C= MANE Select NP_000511.2:n.1526+128C=
NM_001318825.2:c.1559+128C= NP_001305754.1:n.1559+128C=
NR_134869.2:n.1439C=
NR_134869.3:n.1439C=