Canonical Allele Identifier: CA2186743574
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346309C= , CM000677.2:g.72346309C= GRCh38
NC_000015.9:g.72638650C= , CM000677.1:g.72638650C= GRCh37
NC_000015.8:g.70425704C= NCBI36
NG_009017.1:g.34871G=
NG_009017.2:g.34871G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*7G= ENSP00000457521.2:n.*7G=
ENST00000682061.1:c.*1009G= ENSP00000508316.1:n.*1009G=
ENST00000682064.1:n.890G=
ENST00000682177.1:c.1390G= ENSP00000507409.1:n.1390G=
ENST00000682235.1:n.686G=
ENST00000682461.1:c.1453G= ENSP00000507308.1:n.1453G=
ENST00000682653.1:n.1667G=
ENST00000682657.1:c.*500G= ENSP00000507753.1:n.*500G=
ENST00000682721.1:c.*1150G= ENSP00000507535.1:n.*1150G=
ENST00000682843.1:c.*988G= ENSP00000508173.1:n.*988G=
ENST00000683003.1:c.*500G= ENSP00000507576.1:n.*500G=
ENST00000683133.1:c.1531G= ENSP00000508108.1:n.1531G=
ENST00000683243.1:c.*500G= ENSP00000507042.1:n.*500G=
ENST00000683463.1:c.*152G= ENSP00000507986.1:n.*152G=
ENST00000683548.1:n.1121G=
ENST00000683579.1:c.*1245G= ENSP00000506867.1:n.*1245G=
ENST00000683587.1:n.1194G=
ENST00000683681.1:c.1347G= ENSP00000508110.1:p.Lys449=
ENST00000683735.1:c.*1061G= ENSP00000508336.1:n.*1061G=
ENST00000683853.1:c.*152G= ENSP00000506834.1:n.*152G=
ENST00000683860.1:c.1347G= ENSP00000507179.1:p.Lys449=
ENST00000683884.1:c.1163G= ENSP00000507004.1:p.Arg388=
ENST00000684041.1:c.1347G= ENSP00000508382.1:p.Lys449=
ENST00000684125.1:c.*7G= ENSP00000507320.1:n.*7G=
ENST00000684203.1:n.3112G=
ENST00000684231.1:c.*757G= ENSP00000507748.1:n.*757G=
ENST00000684263.1:c.*287G= ENSP00000508369.1:n.*287G=
ENST00000684305.1:c.1795G= ENSP00000506819.1:n.1795G=
ENST00000684415.1:c.*214G= ENSP00000507227.1:n.*214G=
ENST00000684520.1:c.1347G= ENSP00000506826.1:p.Lys449=
ENST00000684602.1:c.*1013G= ENSP00000507996.1:n.*1013G=
ENST00000684667.1:c.1678G= ENSP00000507003.1:n.1678G=
ENST00000268097.10:c.1347G= MANE Select ENSP00000268097.6:p.Lys449=
ENST00000268097.9:c.1347G= ENSP00000268097.5:p.Lys449=
ENST00000379915.4:c.429G= ENSP00000478716.1:p.Lys143=
ENST00000563762.5:c.842G= ENSP00000456346.1:n.842G=
ENST00000566304.5:c.1380G= ENSP00000455114.1:p.Lys460=
ENST00000566672.5:c.*757G= ENSP00000457037.1:n.*757G=
ENST00000567027.5:c.962G=
ENST00000567159.5:c.1347G= ENSP00000456489.1:p.Lys449=
ENST00000567411.5:c.*868G= ENSP00000455545.1:n.*868G=
ENST00000568777.5:n.6567G=
ENST00000569410.5:c.*152G= ENSP00000457125.1:n.*152G=
NM_000520.4:c.1347G= NP_000511.2:p.Lys449=
NM_000520.5:c.1347G= NP_000511.2:p.Lys449=
NM_001318825.1:c.1380G= NP_001305754.1:p.Lys460=
NR_134869.1:n.1591G=
NM_000520.6:c.1347G= MANE Select NP_000511.2:p.Lys449=
NM_001318825.2:c.1380G= NP_001305754.1:p.Lys460=
NR_134869.2:n.1132G=
NR_134869.3:n.1132G=