Canonical Allele Identifier: CA2186743675
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346558A= , CM000677.2:g.72346558A= GRCh38
NC_000015.9:g.72638899A= , CM000677.1:g.72638899A= GRCh37
NC_000015.8:g.70425953A= NCBI36
NG_009017.1:g.34622T=
NG_009017.2:g.34622T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.1074-233T= ENSP00000457521.2:n.1074-233T=
ENST00000682061.1:c.*961T= ENSP00000508316.1:n.*961T=
ENST00000682064.1:n.641T=
ENST00000682177.1:c.1342T= ENSP00000507409.1:n.1342T=
ENST00000682235.1:n.638T=
ENST00000682461.1:c.1405T= ENSP00000507308.1:n.1405T=
ENST00000682653.1:n.1619T=
ENST00000682657.1:c.*484-233T= ENSP00000507753.1:n.*484-233T=
ENST00000682721.1:c.*1102T= ENSP00000507535.1:n.*1102T=
ENST00000682843.1:c.*972-233T= ENSP00000508173.1:n.*972-233T=
ENST00000683003.1:c.*484-233T= ENSP00000507576.1:n.*484-233T=
ENST00000683133.1:c.1483T= ENSP00000508108.1:n.1483T=
ENST00000683243.1:c.*484-233T= ENSP00000507042.1:n.*484-233T=
ENST00000683463.1:c.*104T= ENSP00000507986.1:n.*104T=
ENST00000683548.1:n.1105-233T=
ENST00000683579.1:c.*1197T= ENSP00000506867.1:n.*1197T=
ENST00000683587.1:n.1178-233T=
ENST00000683681.1:c.1299T= ENSP00000508110.1:p.Asp433=
ENST00000683735.1:c.*1045-233T= ENSP00000508336.1:n.*1045-233T=
ENST00000683853.1:c.*104T= ENSP00000506834.1:n.*104T=
ENST00000683860.1:c.1299T= ENSP00000507179.1:p.Asp433=
ENST00000683884.1:c.1147-233T= ENSP00000507004.1:n.1147-233T=
ENST00000684041.1:c.1299T= ENSP00000508382.1:p.Asp433=
ENST00000684125.1:c.1074-233T= ENSP00000507320.1:n.1074-233T=
ENST00000684203.1:n.3064T=
ENST00000684231.1:c.*709T= ENSP00000507748.1:n.*709T=
ENST00000684263.1:c.*239T= ENSP00000508369.1:n.*239T=
ENST00000684305.1:c.1747T= ENSP00000506819.1:n.1747T=
ENST00000684415.1:c.*166T= ENSP00000507227.1:n.*166T=
ENST00000684520.1:c.1299T= ENSP00000506826.1:p.Asp433=
ENST00000684602.1:c.*965T= ENSP00000507996.1:n.*965T=
ENST00000684667.1:c.1630T= ENSP00000507003.1:n.1630T=
ENST00000268097.10:c.1299T= MANE Select ENSP00000268097.6:p.Asp433=
ENST00000268097.9:c.1299T= ENSP00000268097.5:p.Asp433=
ENST00000379915.4:c.413-233T= ENSP00000478716.1:n.413-233T=
ENST00000563762.5:c.826-233T= ENSP00000456346.1:n.826-233T=
ENST00000566304.5:c.1332T= ENSP00000455114.1:p.Asp444=
ENST00000566672.5:c.*709T= ENSP00000457037.1:n.*709T=
ENST00000567027.5:c.946-233T=
ENST00000567159.5:c.1299T= ENSP00000456489.1:p.Asp433=
ENST00000567411.5:c.*820T= ENSP00000455545.1:n.*820T=
ENST00000568777.5:n.6551-233T=
ENST00000569410.5:c.*104T= ENSP00000457125.1:n.*104T=
NM_000520.4:c.1299T= NP_000511.2:p.Asp433=
NM_000520.5:c.1299T= NP_000511.2:p.Asp433=
NM_001318825.1:c.1332T= NP_001305754.1:p.Asp444=
NR_134869.1:n.1575-233T=
NM_000520.6:c.1299T= MANE Select NP_000511.2:p.Asp433=
NM_001318825.2:c.1332T= NP_001305754.1:p.Asp444=
NR_134869.2:n.1116-233T=
NR_134869.3:n.1116-233T=