Canonical Allele Identifier: CA2186743724
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346662T= , CM000677.2:g.72346662T= GRCh38
NC_000015.9:g.72639003T= , CM000677.1:g.72639003T= GRCh37
NC_000015.8:g.70426057T= NCBI36
NG_009017.1:g.34518A=
NG_009017.2:g.34518A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.1074-337A= ENSP00000457521.2:n.1074-337A=
ENST00000682061.1:c.*857A= ENSP00000508316.1:n.*857A=
ENST00000682064.1:n.537A=
ENST00000682177.1:c.1238A= ENSP00000507409.1:n.1238A=
ENST00000682235.1:n.534A=
ENST00000682461.1:c.1301A= ENSP00000507308.1:n.1301A=
ENST00000682653.1:n.1515A=
ENST00000682657.1:c.*484-337A= ENSP00000507753.1:n.*484-337A=
ENST00000682721.1:c.*998A= ENSP00000507535.1:n.*998A=
ENST00000682843.1:c.*972-337A= ENSP00000508173.1:n.*972-337A=
ENST00000683003.1:c.*484-337A= ENSP00000507576.1:n.*484-337A=
ENST00000683133.1:c.1379A= ENSP00000508108.1:n.1379A=
ENST00000683243.1:c.*484-337A= ENSP00000507042.1:n.*484-337A=
ENST00000683463.1:c.1122A= ENSP00000507986.1:p.Ter374=
ENST00000683548.1:n.1105-337A=
ENST00000683579.1:c.*1093A= ENSP00000506867.1:n.*1093A=
ENST00000683587.1:n.1178-337A=
ENST00000683681.1:c.1195A= ENSP00000508110.1:p.Asn399=
ENST00000683735.1:c.*1045-337A= ENSP00000508336.1:n.*1045-337A=
ENST00000683853.1:c.1122A= ENSP00000506834.1:p.Ter374=
ENST00000683860.1:c.1195A= ENSP00000507179.1:p.Asn399=
ENST00000683884.1:c.1147-337A= ENSP00000507004.1:n.1147-337A=
ENST00000684041.1:c.1195A= ENSP00000508382.1:p.Asn399=
ENST00000684125.1:c.1074-337A= ENSP00000507320.1:n.1074-337A=
ENST00000684203.1:n.2960A=
ENST00000684231.1:c.*605A= ENSP00000507748.1:n.*605A=
ENST00000684263.1:c.*135A= ENSP00000508369.1:n.*135A=
ENST00000684305.1:c.1643A= ENSP00000506819.1:n.1643A=
ENST00000684415.1:c.*62A= ENSP00000507227.1:n.*62A=
ENST00000684520.1:c.1195A= ENSP00000506826.1:p.Asn399=
ENST00000684602.1:c.*861A= ENSP00000507996.1:n.*861A=
ENST00000684667.1:c.1526A= ENSP00000507003.1:n.1526A=
ENST00000268097.10:c.1195A= MANE Select ENSP00000268097.6:p.Asn399=
ENST00000268097.9:c.1195A= ENSP00000268097.5:p.Asn399=
ENST00000379915.4:c.413-337A= ENSP00000478716.1:n.413-337A=
ENST00000563762.5:c.826-337A= ENSP00000456346.1:n.826-337A=
ENST00000566304.5:c.1228A= ENSP00000455114.1:p.Asn410=
ENST00000566672.5:c.*605A= ENSP00000457037.1:n.*605A=
ENST00000567027.5:c.946-337A=
ENST00000567159.5:c.1195A= ENSP00000456489.1:p.Asn399=
ENST00000567411.5:c.*716A= ENSP00000455545.1:n.*716A=
ENST00000568777.5:n.6551-337A=
ENST00000569410.5:c.1122A= ENSP00000457125.1:p.Ter374=
NM_000520.4:c.1195A= NP_000511.2:p.Asn399=
NM_000520.5:c.1195A= NP_000511.2:p.Asn399=
NM_001318825.1:c.1228A= NP_001305754.1:p.Asn410=
NR_134869.1:n.1575-337A=
NM_000520.6:c.1195A= MANE Select NP_000511.2:p.Asn399=
NM_001318825.2:c.1228A= NP_001305754.1:p.Asn410=
NR_134869.2:n.1116-337A=
NR_134869.3:n.1116-337A=