Canonical Allele Identifier: CA2186743188
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345323A= , CM000677.2:g.72345323A= GRCh38
NC_000015.9:g.72637664A= , CM000677.1:g.72637664A= GRCh37
NC_000015.8:g.70424718A= NCBI36
NG_009017.1:g.35857T=
NG_009017.2:g.35857T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*309T= ENSP00000457521.2:n.*309T=
ENST00000682061.1:c.*1995T= ENSP00000508316.1:n.*1995T=
ENST00000682064.1:n.1753+123T=
ENST00000682177.1:c.1692T= ENSP00000507409.1:n.1692T=
ENST00000682235.1:n.1549+123T=
ENST00000682461.1:c.1632+123T= ENSP00000507308.1:n.1632+123T=
ENST00000682653.1:n.2653T=
ENST00000682657.1:c.*1486T= ENSP00000507753.1:n.*1486T=
ENST00000682721.1:c.*1329+123T= ENSP00000507535.1:n.*1329+123T=
ENST00000682843.1:c.*1167+123T= ENSP00000508173.1:n.*1167+123T=
ENST00000683133.1:c.1710+123T= ENSP00000508108.1:n.1710+123T=
ENST00000683243.1:c.*679+123T= ENSP00000507042.1:n.*679+123T=
ENST00000683463.1:c.*1015+123T= ENSP00000507986.1:n.*1015+123T=
ENST00000683548.1:n.1984+123T=
ENST00000683579.1:c.*1424+123T= ENSP00000506867.1:n.*1424+123T=
ENST00000683587.1:n.2057+123T=
ENST00000683681.1:c.*204+123T= ENSP00000508110.1:n.*204+123T=
ENST00000683735.1:c.*1924+123T= ENSP00000508336.1:n.*1924+123T=
ENST00000683853.1:c.*454T= ENSP00000506834.1:n.*454T=
ENST00000683860.1:c.*646+123T= ENSP00000507179.1:n.*646+123T=
ENST00000683884.1:c.*976T= ENSP00000507004.1:n.*976T=
ENST00000684125.1:c.*186+123T= ENSP00000507320.1:n.*186+123T=
ENST00000684203.1:n.3975+123T=
ENST00000684231.1:c.*936+123T= ENSP00000507748.1:n.*936+123T=
ENST00000684263.1:c.*1150+123T= ENSP00000508369.1:n.*1150+123T=
ENST00000684305.1:c.1974+123T= ENSP00000506819.1:n.1974+123T=
ENST00000684415.1:c.*1200T= ENSP00000507227.1:n.*1200T=
ENST00000684520.1:c.*908T= ENSP00000506826.1:n.*908T=
ENST00000684602.1:c.*1192+123T= ENSP00000507996.1:n.*1192+123T=
ENST00000684667.1:c.1857+123T= ENSP00000507003.1:n.1857+123T=
ENST00000268097.10:c.1526+123T= MANE Select ENSP00000268097.6:n.1526+123T=
ENST00000268097.9:c.1526+123T= ENSP00000268097.5:n.1526+123T=
ENST00000379915.4:c.608+123T= ENSP00000478716.1:n.608+123T=
ENST00000564677.5:n.318+123T=
ENST00000565873.1:n.437+123T=
ENST00000566304.5:c.1559+123T= ENSP00000455114.1:n.1559+123T=
ENST00000567027.5:c.1264T=
ENST00000567411.5:c.*1047+123T= ENSP00000455545.1:n.*1047+123T=
ENST00000568777.5:n.6869T=
ENST00000569116.1:n.356T=
NM_000520.4:c.1526+123T= NP_000511.2:n.1526+123T=
NM_000520.5:c.1526+123T= NP_000511.2:n.1526+123T=
NM_001318825.1:c.1559+123T= NP_001305754.1:n.1559+123T=
NR_134869.1:n.1893T=
NM_000520.6:c.1526+123T= MANE Select NP_000511.2:n.1526+123T=
NM_001318825.2:c.1559+123T= NP_001305754.1:n.1559+123T=
NR_134869.2:n.1434T=
NR_134869.3:n.1434T=