Canonical Allele Identifier: CA2186743745
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346701C= , CM000677.2:g.72346701C= GRCh38
NC_000015.9:g.72639042C= , CM000677.1:g.72639042C= GRCh37
NC_000015.8:g.70426096C= NCBI36
NG_009017.1:g.34479G=
NG_009017.2:g.34479G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.1074-376G= ENSP00000457521.2:n.1074-376G=
ENST00000682061.1:c.*818G= ENSP00000508316.1:n.*818G=
ENST00000682064.1:n.498G=
ENST00000682177.1:c.1199G= ENSP00000507409.1:n.1199G=
ENST00000682235.1:n.495G=
ENST00000682461.1:c.1262G= ENSP00000507308.1:n.1262G=
ENST00000682653.1:n.1476G=
ENST00000682657.1:c.*484-376G= ENSP00000507753.1:n.*484-376G=
ENST00000682721.1:c.*959G= ENSP00000507535.1:n.*959G=
ENST00000682843.1:c.*972-376G= ENSP00000508173.1:n.*972-376G=
ENST00000683003.1:c.*484-376G= ENSP00000507576.1:n.*484-376G=
ENST00000683133.1:c.1340G= ENSP00000508108.1:n.1340G=
ENST00000683243.1:c.*484-376G= ENSP00000507042.1:n.*484-376G=
ENST00000683463.1:c.1083G= ENSP00000507986.1:p.Gln361=
ENST00000683548.1:n.1105-376G=
ENST00000683579.1:c.*1054G= ENSP00000506867.1:n.*1054G=
ENST00000683587.1:n.1178-376G=
ENST00000683681.1:c.1156G= ENSP00000508110.1:p.Asp386=
ENST00000683735.1:c.*1045-376G= ENSP00000508336.1:n.*1045-376G=
ENST00000683853.1:c.1083G= ENSP00000506834.1:p.Gln361=
ENST00000683860.1:c.1156G= ENSP00000507179.1:p.Asp386=
ENST00000683884.1:c.1147-376G= ENSP00000507004.1:n.1147-376G=
ENST00000684041.1:c.1156G= ENSP00000508382.1:p.Asp386=
ENST00000684125.1:c.1074-376G= ENSP00000507320.1:n.1074-376G=
ENST00000684203.1:n.2921G=
ENST00000684231.1:c.*566G= ENSP00000507748.1:n.*566G=
ENST00000684263.1:c.*96G= ENSP00000508369.1:n.*96G=
ENST00000684305.1:c.1604G= ENSP00000506819.1:n.1604G=
ENST00000684415.1:c.*23G= ENSP00000507227.1:n.*23G=
ENST00000684520.1:c.1156G= ENSP00000506826.1:p.Asp386=
ENST00000684602.1:c.*822G= ENSP00000507996.1:n.*822G=
ENST00000684667.1:c.1487G= ENSP00000507003.1:n.1487G=
ENST00000268097.10:c.1156G= MANE Select ENSP00000268097.6:p.Asp386=
ENST00000268097.9:c.1156G= ENSP00000268097.5:p.Asp386=
ENST00000379915.4:c.413-376G= ENSP00000478716.1:n.413-376G=
ENST00000563762.5:c.826-376G= ENSP00000456346.1:n.826-376G=
ENST00000566304.5:c.1189G= ENSP00000455114.1:p.Asp397=
ENST00000566672.5:c.*566G= ENSP00000457037.1:n.*566G=
ENST00000567027.5:c.946-376G=
ENST00000567159.5:c.1156G= ENSP00000456489.1:p.Asp386=
ENST00000567411.5:c.*677G= ENSP00000455545.1:n.*677G=
ENST00000568777.5:n.6551-376G=
ENST00000569410.5:c.1083G= ENSP00000457125.1:p.Gln361=
NM_000520.4:c.1156G= NP_000511.2:p.Asp386=
NM_000520.5:c.1156G= NP_000511.2:p.Asp386=
NM_001318825.1:c.1189G= NP_001305754.1:p.Asp397=
NR_134869.1:n.1575-376G=
NM_000520.6:c.1156G= MANE Select NP_000511.2:p.Asp386=
NM_001318825.2:c.1189G= NP_001305754.1:p.Asp397=
NR_134869.2:n.1116-376G=
NR_134869.3:n.1116-376G=