Canonical Allele Identifier: CA2186743256
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345455T= , CM000677.2:g.72345455T= GRCh38
NC_000015.9:g.72637796T= , CM000677.1:g.72637796T= GRCh37
NC_000015.8:g.70424850T= NCBI36
NG_009017.1:g.35725A=
NG_009017.2:g.35725A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*177A= ENSP00000457521.2:n.*177A=
ENST00000682061.1:c.*1863A= ENSP00000508316.1:n.*1863A=
ENST00000682064.1:n.1744A=
ENST00000682177.1:c.1560A= ENSP00000507409.1:n.1560A=
ENST00000682235.1:n.1540A=
ENST00000682461.1:c.1623A= ENSP00000507308.1:n.1623A=
ENST00000682653.1:n.2521A=
ENST00000682657.1:c.*1354A= ENSP00000507753.1:n.*1354A=
ENST00000682721.1:c.*1320A= ENSP00000507535.1:n.*1320A=
ENST00000682843.1:c.*1158A= ENSP00000508173.1:n.*1158A=
ENST00000683003.1:c.*1354A= ENSP00000507576.1:n.*1354A=
ENST00000683133.1:c.1701A= ENSP00000508108.1:n.1701A=
ENST00000683243.1:c.*670A= ENSP00000507042.1:n.*670A=
ENST00000683463.1:c.*1006A= ENSP00000507986.1:n.*1006A=
ENST00000683548.1:n.1975A=
ENST00000683579.1:c.*1415A= ENSP00000506867.1:n.*1415A=
ENST00000683587.1:n.2048A=
ENST00000683681.1:c.*195A= ENSP00000508110.1:n.*195A=
ENST00000683735.1:c.*1915A= ENSP00000508336.1:n.*1915A=
ENST00000683853.1:c.*322A= ENSP00000506834.1:n.*322A=
ENST00000683860.1:c.*637A= ENSP00000507179.1:n.*637A=
ENST00000683884.1:c.*844A= ENSP00000507004.1:n.*844A=
ENST00000684125.1:c.*177A= ENSP00000507320.1:n.*177A=
ENST00000684203.1:n.3966A=
ENST00000684231.1:c.*927A= ENSP00000507748.1:n.*927A=
ENST00000684263.1:c.*1141A= ENSP00000508369.1:n.*1141A=
ENST00000684305.1:c.1965A= ENSP00000506819.1:n.1965A=
ENST00000684415.1:c.*1068A= ENSP00000507227.1:n.*1068A=
ENST00000684520.1:c.*776A= ENSP00000506826.1:n.*776A=
ENST00000684602.1:c.*1183A= ENSP00000507996.1:n.*1183A=
ENST00000684667.1:c.1848A= ENSP00000507003.1:n.1848A=
ENST00000268097.10:c.1517A= MANE Select ENSP00000268097.6:p.Glu506=
ENST00000268097.9:c.1517A= ENSP00000268097.5:p.Glu506=
ENST00000379915.4:c.599A= ENSP00000478716.1:p.Glu200=
ENST00000564677.5:n.309A=
ENST00000565873.1:n.428A=
ENST00000566304.5:c.1550A= ENSP00000455114.1:p.Glu517=
ENST00000567027.5:c.1132A=
ENST00000567159.5:c.1517A= ENSP00000456489.1:p.Glu506=
ENST00000567411.5:c.*1038A= ENSP00000455545.1:n.*1038A=
ENST00000568777.5:n.6737A=
ENST00000569116.1:n.224A=
NM_000520.4:c.1517A= NP_000511.2:p.Glu506=
NM_000520.5:c.1517A= NP_000511.2:p.Glu506=
NM_001318825.1:c.1550A= NP_001305754.1:p.Glu517=
NR_134869.1:n.1761A=
NM_000520.6:c.1517A= MANE Select NP_000511.2:p.Glu506=
NM_001318825.2:c.1550A= NP_001305754.1:p.Glu517=
NR_134869.2:n.1302A=
NR_134869.3:n.1302A=