Canonical Allele Identifier: CA2186743251
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345441C= , CM000677.2:g.72345441C= GRCh38
NC_000015.9:g.72637782C= , CM000677.1:g.72637782C= GRCh37
NC_000015.8:g.70424836C= NCBI36
NG_009017.1:g.35739G=
NG_009017.2:g.35739G=

Transcript Alleles

HGVS Amino-acid change
ENST00000567027.6:c.*191G= ENSP00000457521.2:n.*191G=
ENST00000682061.1:c.*1877G= ENSP00000508316.1:n.*1877G=
ENST00000682064.1:n.1753+5G=
ENST00000682177.1:c.1574G= ENSP00000507409.1:n.1574G=
ENST00000682235.1:n.1549+5G=
ENST00000682461.1:c.1632+5G= ENSP00000507308.1:n.1632+5G=
ENST00000682653.1:n.2535G=
ENST00000682657.1:c.*1368G= ENSP00000507753.1:n.*1368G=
ENST00000682721.1:c.*1329+5G= ENSP00000507535.1:n.*1329+5G=
ENST00000682843.1:c.*1167+5G= ENSP00000508173.1:n.*1167+5G=
ENST00000683003.1:c.*1368G= ENSP00000507576.1:n.*1368G=
ENST00000683133.1:c.1710+5G= ENSP00000508108.1:n.1710+5G=
ENST00000683243.1:c.*679+5G= ENSP00000507042.1:n.*679+5G=
ENST00000683463.1:c.*1015+5G= ENSP00000507986.1:n.*1015+5G=
ENST00000683548.1:n.1984+5G=
ENST00000683579.1:c.*1424+5G= ENSP00000506867.1:n.*1424+5G=
ENST00000683587.1:n.2057+5G=
ENST00000683681.1:c.*204+5G= ENSP00000508110.1:n.*204+5G=
ENST00000683735.1:c.*1924+5G= ENSP00000508336.1:n.*1924+5G=
ENST00000683853.1:c.*336G= ENSP00000506834.1:n.*336G=
ENST00000683860.1:c.*646+5G= ENSP00000507179.1:n.*646+5G=
ENST00000683884.1:c.*858G= ENSP00000507004.1:n.*858G=
ENST00000684125.1:c.*186+5G= ENSP00000507320.1:n.*186+5G=
ENST00000684203.1:n.3975+5G=
ENST00000684231.1:c.*936+5G= ENSP00000507748.1:n.*936+5G=
ENST00000684263.1:c.*1150+5G= ENSP00000508369.1:n.*1150+5G=
ENST00000684305.1:c.1974+5G= ENSP00000506819.1:n.1974+5G=
ENST00000684415.1:c.*1082G= ENSP00000507227.1:n.*1082G=
ENST00000684520.1:c.*790G= ENSP00000506826.1:n.*790G=
ENST00000684602.1:c.*1192+5G= ENSP00000507996.1:n.*1192+5G=
ENST00000684667.1:c.1857+5G= ENSP00000507003.1:n.1857+5G=
ENST00000268097.10:c.1526+5G= MANE Select ENSP00000268097.6:n.1526+5G=
ENST00000268097.9:c.1526+5G= ENSP00000268097.5:n.1526+5G=
ENST00000379915.4:c.608+5G= ENSP00000478716.1:n.608+5G=
ENST00000564677.5:n.318+5G=
ENST00000565873.1:n.437+5G=
ENST00000566304.5:c.1559+5G= ENSP00000455114.1:n.1559+5G=
ENST00000567027.5:c.1146G=
ENST00000567159.5:c.*1G= ENSP00000456489.1:n.*1G=
ENST00000567411.5:c.*1047+5G= ENSP00000455545.1:n.*1047+5G=
ENST00000568777.5:n.6751G=
ENST00000569116.1:n.238G=
NM_000520.4:c.1526+5G= NP_000511.2:n.1526+5G=
NM_000520.5:c.1526+5G= NP_000511.2:n.1526+5G=
NM_001318825.1:c.1559+5G= NP_001305754.1:n.1559+5G=
NR_134869.1:n.1775G=
NM_000520.6:c.1526+5G= MANE Select NP_000511.2:n.1526+5G=
NM_001318825.2:c.1559+5G= NP_001305754.1:n.1559+5G=
NR_134869.2:n.1316G=
NR_134869.3:n.1316G=