Canonical Allele Identifier: CA2186743235
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345407G= , CM000677.2:g.72345407G= GRCh38
NC_000015.9:g.72637748G= , CM000677.1:g.72637748G= GRCh37
NC_000015.8:g.70424802G= NCBI36
NG_009017.1:g.35773C=
NG_009017.2:g.35773C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*225C= ENSP00000457521.2:n.*225C=
ENST00000682061.1:c.*1911C= ENSP00000508316.1:n.*1911C=
ENST00000682064.1:n.1753+39C=
ENST00000682177.1:c.1608C= ENSP00000507409.1:n.1608C=
ENST00000682235.1:n.1549+39C=
ENST00000682461.1:c.1632+39C= ENSP00000507308.1:n.1632+39C=
ENST00000682653.1:n.2569C=
ENST00000682657.1:c.*1402C= ENSP00000507753.1:n.*1402C=
ENST00000682721.1:c.*1329+39C= ENSP00000507535.1:n.*1329+39C=
ENST00000682843.1:c.*1167+39C= ENSP00000508173.1:n.*1167+39C=
ENST00000683003.1:c.*1402C= ENSP00000507576.1:n.*1402C=
ENST00000683133.1:c.1710+39C= ENSP00000508108.1:n.1710+39C=
ENST00000683243.1:c.*679+39C= ENSP00000507042.1:n.*679+39C=
ENST00000683463.1:c.*1015+39C= ENSP00000507986.1:n.*1015+39C=
ENST00000683548.1:n.1984+39C=
ENST00000683579.1:c.*1424+39C= ENSP00000506867.1:n.*1424+39C=
ENST00000683587.1:n.2057+39C=
ENST00000683681.1:c.*204+39C= ENSP00000508110.1:n.*204+39C=
ENST00000683735.1:c.*1924+39C= ENSP00000508336.1:n.*1924+39C=
ENST00000683853.1:c.*370C= ENSP00000506834.1:n.*370C=
ENST00000683860.1:c.*646+39C= ENSP00000507179.1:n.*646+39C=
ENST00000683884.1:c.*892C= ENSP00000507004.1:n.*892C=
ENST00000684125.1:c.*186+39C= ENSP00000507320.1:n.*186+39C=
ENST00000684203.1:n.3975+39C=
ENST00000684231.1:c.*936+39C= ENSP00000507748.1:n.*936+39C=
ENST00000684263.1:c.*1150+39C= ENSP00000508369.1:n.*1150+39C=
ENST00000684305.1:c.1974+39C= ENSP00000506819.1:n.1974+39C=
ENST00000684415.1:c.*1116C= ENSP00000507227.1:n.*1116C=
ENST00000684520.1:c.*824C= ENSP00000506826.1:n.*824C=
ENST00000684602.1:c.*1192+39C= ENSP00000507996.1:n.*1192+39C=
ENST00000684667.1:c.1857+39C= ENSP00000507003.1:n.1857+39C=
ENST00000268097.10:c.1526+39C= MANE Select ENSP00000268097.6:n.1526+39C=
ENST00000268097.9:c.1526+39C= ENSP00000268097.5:n.1526+39C=
ENST00000379915.4:c.608+39C= ENSP00000478716.1:n.608+39C=
ENST00000564677.5:n.318+39C=
ENST00000565873.1:n.437+39C=
ENST00000566304.5:c.1559+39C= ENSP00000455114.1:n.1559+39C=
ENST00000567027.5:c.1180C=
ENST00000567411.5:c.*1047+39C= ENSP00000455545.1:n.*1047+39C=
ENST00000568777.5:n.6785C=
ENST00000569116.1:n.272C=
NM_000520.4:c.1526+39C= NP_000511.2:n.1526+39C=
NM_000520.5:c.1526+39C= NP_000511.2:n.1526+39C=
NM_001318825.1:c.1559+39C= NP_001305754.1:n.1559+39C=
NR_134869.1:n.1809C=
NM_000520.6:c.1526+39C= MANE Select NP_000511.2:n.1526+39C=
NM_001318825.2:c.1559+39C= NP_001305754.1:n.1559+39C=
NR_134869.2:n.1350C=
NR_134869.3:n.1350C=