Canonical Allele Identifier: CA2186743259
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345462G= , CM000677.2:g.72345462G= GRCh38
NC_000015.9:g.72637803G= , CM000677.1:g.72637803G= GRCh37
NC_000015.8:g.70424857G= NCBI36
NG_009017.1:g.35718C=
NG_009017.2:g.35718C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*170C= ENSP00000457521.2:n.*170C=
ENST00000682061.1:c.*1856C= ENSP00000508316.1:n.*1856C=
ENST00000682064.1:n.1737C=
ENST00000682177.1:c.1553C= ENSP00000507409.1:n.1553C=
ENST00000682235.1:n.1533C=
ENST00000682461.1:c.1616C= ENSP00000507308.1:n.1616C=
ENST00000682653.1:n.2514C=
ENST00000682657.1:c.*1347C= ENSP00000507753.1:n.*1347C=
ENST00000682721.1:c.*1313C= ENSP00000507535.1:n.*1313C=
ENST00000682843.1:c.*1151C= ENSP00000508173.1:n.*1151C=
ENST00000683003.1:c.*1347C= ENSP00000507576.1:n.*1347C=
ENST00000683133.1:c.1694C= ENSP00000508108.1:n.1694C=
ENST00000683243.1:c.*663C= ENSP00000507042.1:n.*663C=
ENST00000683463.1:c.*999C= ENSP00000507986.1:n.*999C=
ENST00000683548.1:n.1968C=
ENST00000683579.1:c.*1408C= ENSP00000506867.1:n.*1408C=
ENST00000683587.1:n.2041C=
ENST00000683681.1:c.*188C= ENSP00000508110.1:n.*188C=
ENST00000683735.1:c.*1908C= ENSP00000508336.1:n.*1908C=
ENST00000683853.1:c.*315C= ENSP00000506834.1:n.*315C=
ENST00000683860.1:c.*630C= ENSP00000507179.1:n.*630C=
ENST00000683884.1:c.*837C= ENSP00000507004.1:n.*837C=
ENST00000684125.1:c.*170C= ENSP00000507320.1:n.*170C=
ENST00000684203.1:n.3959C=
ENST00000684231.1:c.*920C= ENSP00000507748.1:n.*920C=
ENST00000684263.1:c.*1134C= ENSP00000508369.1:n.*1134C=
ENST00000684305.1:c.1958C= ENSP00000506819.1:n.1958C=
ENST00000684415.1:c.*1061C= ENSP00000507227.1:n.*1061C=
ENST00000684520.1:c.*769C= ENSP00000506826.1:n.*769C=
ENST00000684602.1:c.*1176C= ENSP00000507996.1:n.*1176C=
ENST00000684667.1:c.1841C= ENSP00000507003.1:n.1841C=
ENST00000268097.10:c.1510C= MANE Select ENSP00000268097.6:p.Arg504=
ENST00000268097.9:c.1510C= ENSP00000268097.5:p.Arg504=
ENST00000379915.4:c.592C= ENSP00000478716.1:p.Arg198=
ENST00000564677.5:n.302C=
ENST00000565873.1:n.421C=
ENST00000566304.5:c.1543C= ENSP00000455114.1:p.Arg515=
ENST00000567027.5:c.1125C=
ENST00000567159.5:c.1510C= ENSP00000456489.1:p.Arg504=
ENST00000567411.5:c.*1031C= ENSP00000455545.1:n.*1031C=
ENST00000568777.5:n.6730C=
ENST00000569116.1:n.217C=
NM_000520.4:c.1510C= NP_000511.2:p.Arg504=
NM_000520.5:c.1510C= NP_000511.2:p.Arg504=
NM_001318825.1:c.1543C= NP_001305754.1:p.Arg515=
NR_134869.1:n.1754C=
NM_000520.6:c.1510C= MANE Select NP_000511.2:p.Arg504=
NM_001318825.2:c.1543C= NP_001305754.1:p.Arg515=
NR_134869.2:n.1295C=
NR_134869.3:n.1295C=