Canonical Allele Identifier: CA2186743577
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346317C= , CM000677.2:g.72346317C= GRCh38
NC_000015.9:g.72638658C= , CM000677.1:g.72638658C= GRCh37
NC_000015.8:g.70425712C= NCBI36
NG_009017.1:g.34863G=
NG_009017.2:g.34863G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.1082G= ENSP00000457521.2:p.Ter361=
ENST00000682061.1:c.*1001G= ENSP00000508316.1:n.*1001G=
ENST00000682064.1:n.882G=
ENST00000682177.1:c.1382G= ENSP00000507409.1:n.1382G=
ENST00000682235.1:n.678G=
ENST00000682461.1:c.1445G= ENSP00000507308.1:n.1445G=
ENST00000682653.1:n.1659G=
ENST00000682657.1:c.*492G= ENSP00000507753.1:n.*492G=
ENST00000682721.1:c.*1142G= ENSP00000507535.1:n.*1142G=
ENST00000682843.1:c.*980G= ENSP00000508173.1:n.*980G=
ENST00000683003.1:c.*492G= ENSP00000507576.1:n.*492G=
ENST00000683133.1:c.1523G= ENSP00000508108.1:n.1523G=
ENST00000683243.1:c.*492G= ENSP00000507042.1:n.*492G=
ENST00000683463.1:c.*144G= ENSP00000507986.1:n.*144G=
ENST00000683548.1:n.1113G=
ENST00000683579.1:c.*1237G= ENSP00000506867.1:n.*1237G=
ENST00000683587.1:n.1186G=
ENST00000683681.1:c.1339G= ENSP00000508110.1:p.Glu447=
ENST00000683735.1:c.*1053G= ENSP00000508336.1:n.*1053G=
ENST00000683853.1:c.*144G= ENSP00000506834.1:n.*144G=
ENST00000683860.1:c.1339G= ENSP00000507179.1:p.Glu447=
ENST00000683884.1:c.1155G= ENSP00000507004.1:p.Leu385=
ENST00000684041.1:c.1339G= ENSP00000508382.1:p.Glu447=
ENST00000684125.1:c.1082G= ENSP00000507320.1:p.Ter361=
ENST00000684203.1:n.3104G=
ENST00000684231.1:c.*749G= ENSP00000507748.1:n.*749G=
ENST00000684263.1:c.*279G= ENSP00000508369.1:n.*279G=
ENST00000684305.1:c.1787G= ENSP00000506819.1:n.1787G=
ENST00000684415.1:c.*206G= ENSP00000507227.1:n.*206G=
ENST00000684520.1:c.1339G= ENSP00000506826.1:p.Glu447=
ENST00000684602.1:c.*1005G= ENSP00000507996.1:n.*1005G=
ENST00000684667.1:c.1670G= ENSP00000507003.1:n.1670G=
ENST00000268097.10:c.1339G= MANE Select ENSP00000268097.6:p.Glu447=
ENST00000268097.9:c.1339G= ENSP00000268097.5:p.Glu447=
ENST00000379915.4:c.421G= ENSP00000478716.1:p.Glu141=
ENST00000563762.5:c.834G= ENSP00000456346.1:n.834G=
ENST00000566304.5:c.1372G= ENSP00000455114.1:p.Glu458=
ENST00000566672.5:c.*749G= ENSP00000457037.1:n.*749G=
ENST00000567027.5:c.954G=
ENST00000567159.5:c.1339G= ENSP00000456489.1:p.Glu447=
ENST00000567411.5:c.*860G= ENSP00000455545.1:n.*860G=
ENST00000568777.5:n.6559G=
ENST00000569410.5:c.*144G= ENSP00000457125.1:n.*144G=
NM_000520.4:c.1339G= NP_000511.2:p.Glu447=
NM_000520.5:c.1339G= NP_000511.2:p.Glu447=
NM_001318825.1:c.1372G= NP_001305754.1:p.Glu458=
NR_134869.1:n.1583G=
NM_000520.6:c.1339G= MANE Select NP_000511.2:p.Glu447=
NM_001318825.2:c.1372G= NP_001305754.1:p.Glu458=
NR_134869.2:n.1124G=
NR_134869.3:n.1124G=