Canonical Allele Identifier: CA2186743684
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346582T= , CM000677.2:g.72346582T= GRCh38
NC_000015.9:g.72638923T= , CM000677.1:g.72638923T= GRCh37
NC_000015.8:g.70425977T= NCBI36
NG_009017.1:g.34598A=
NG_009017.2:g.34598A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.1074-257A= ENSP00000457521.2:n.1074-257A=
ENST00000682061.1:c.*937A= ENSP00000508316.1:n.*937A=
ENST00000682064.1:n.617A=
ENST00000682177.1:c.1318A= ENSP00000507409.1:n.1318A=
ENST00000682235.1:n.614A=
ENST00000682461.1:c.1381A= ENSP00000507308.1:n.1381A=
ENST00000682653.1:n.1595A=
ENST00000682657.1:c.*484-257A= ENSP00000507753.1:n.*484-257A=
ENST00000682721.1:c.*1078A= ENSP00000507535.1:n.*1078A=
ENST00000682843.1:c.*972-257A= ENSP00000508173.1:n.*972-257A=
ENST00000683003.1:c.*484-257A= ENSP00000507576.1:n.*484-257A=
ENST00000683133.1:c.1459A= ENSP00000508108.1:n.1459A=
ENST00000683243.1:c.*484-257A= ENSP00000507042.1:n.*484-257A=
ENST00000683463.1:c.*80A= ENSP00000507986.1:n.*80A=
ENST00000683548.1:n.1105-257A=
ENST00000683579.1:c.*1173A= ENSP00000506867.1:n.*1173A=
ENST00000683587.1:n.1178-257A=
ENST00000683681.1:c.1275A= ENSP00000508110.1:p.Ile425=
ENST00000683735.1:c.*1045-257A= ENSP00000508336.1:n.*1045-257A=
ENST00000683853.1:c.*80A= ENSP00000506834.1:n.*80A=
ENST00000683860.1:c.1275A= ENSP00000507179.1:p.Ile425=
ENST00000683884.1:c.1147-257A= ENSP00000507004.1:n.1147-257A=
ENST00000684041.1:c.1275A= ENSP00000508382.1:p.Ile425=
ENST00000684125.1:c.1074-257A= ENSP00000507320.1:n.1074-257A=
ENST00000684203.1:n.3040A=
ENST00000684231.1:c.*685A= ENSP00000507748.1:n.*685A=
ENST00000684263.1:c.*215A= ENSP00000508369.1:n.*215A=
ENST00000684305.1:c.1723A= ENSP00000506819.1:n.1723A=
ENST00000684415.1:c.*142A= ENSP00000507227.1:n.*142A=
ENST00000684520.1:c.1275A= ENSP00000506826.1:p.Ile425=
ENST00000684602.1:c.*941A= ENSP00000507996.1:n.*941A=
ENST00000684667.1:c.1606A= ENSP00000507003.1:n.1606A=
ENST00000268097.10:c.1275A= MANE Select ENSP00000268097.6:p.Ile425=
ENST00000268097.9:c.1275A= ENSP00000268097.5:p.Ile425=
ENST00000379915.4:c.413-257A= ENSP00000478716.1:n.413-257A=
ENST00000563762.5:c.826-257A= ENSP00000456346.1:n.826-257A=
ENST00000566304.5:c.1308A= ENSP00000455114.1:p.Ile436=
ENST00000566672.5:c.*685A= ENSP00000457037.1:n.*685A=
ENST00000567027.5:c.946-257A=
ENST00000567159.5:c.1275A= ENSP00000456489.1:p.Ile425=
ENST00000567411.5:c.*796A= ENSP00000455545.1:n.*796A=
ENST00000568777.5:n.6551-257A=
ENST00000569410.5:c.*80A= ENSP00000457125.1:n.*80A=
NM_000520.4:c.1275A= NP_000511.2:p.Ile425=
NM_000520.5:c.1275A= NP_000511.2:p.Ile425=
NM_001318825.1:c.1308A= NP_001305754.1:p.Ile436=
NR_134869.1:n.1575-257A=
NM_000520.6:c.1275A= MANE Select NP_000511.2:p.Ile425=
NM_001318825.2:c.1308A= NP_001305754.1:p.Ile436=
NR_134869.2:n.1116-257A=
NR_134869.3:n.1116-257A=