Canonical Allele Identifier: CA2186743273
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345495G= , CM000677.2:g.72345495G= GRCh38
NC_000015.9:g.72637836G= , CM000677.1:g.72637836G= GRCh37
NC_000015.8:g.70424890G= NCBI36
NG_009017.1:g.35685C=
NG_009017.2:g.35685C=

Transcript Alleles

HGVS Amino-acid change
ENST00000567027.6:c.*137C= ENSP00000457521.2:n.*137C=
ENST00000682061.1:c.*1823C= ENSP00000508316.1:n.*1823C=
ENST00000682064.1:n.1704C=
ENST00000682177.1:c.1520C= ENSP00000507409.1:n.1520C=
ENST00000682235.1:n.1500C=
ENST00000682461.1:c.1583C= ENSP00000507308.1:n.1583C=
ENST00000682653.1:n.2481C=
ENST00000682657.1:c.*1314C= ENSP00000507753.1:n.*1314C=
ENST00000682721.1:c.*1280C= ENSP00000507535.1:n.*1280C=
ENST00000682843.1:c.*1118C= ENSP00000508173.1:n.*1118C=
ENST00000683003.1:c.*1314C= ENSP00000507576.1:n.*1314C=
ENST00000683133.1:c.1661C= ENSP00000508108.1:n.1661C=
ENST00000683243.1:c.*630C= ENSP00000507042.1:n.*630C=
ENST00000683463.1:c.*966C= ENSP00000507986.1:n.*966C=
ENST00000683548.1:n.1935C=
ENST00000683579.1:c.*1375C= ENSP00000506867.1:n.*1375C=
ENST00000683587.1:n.2008C=
ENST00000683681.1:c.*155C= ENSP00000508110.1:n.*155C=
ENST00000683735.1:c.*1875C= ENSP00000508336.1:n.*1875C=
ENST00000683853.1:c.*282C= ENSP00000506834.1:n.*282C=
ENST00000683860.1:c.*597C= ENSP00000507179.1:n.*597C=
ENST00000683884.1:c.*804C= ENSP00000507004.1:n.*804C=
ENST00000684041.1:c.*610C= ENSP00000508382.1:n.*610C=
ENST00000684125.1:c.*137C= ENSP00000507320.1:n.*137C=
ENST00000684203.1:n.3926C=
ENST00000684231.1:c.*887C= ENSP00000507748.1:n.*887C=
ENST00000684263.1:c.*1101C= ENSP00000508369.1:n.*1101C=
ENST00000684305.1:c.1925C= ENSP00000506819.1:n.1925C=
ENST00000684415.1:c.*1028C= ENSP00000507227.1:n.*1028C=
ENST00000684520.1:c.*736C= ENSP00000506826.1:n.*736C=
ENST00000684602.1:c.*1143C= ENSP00000507996.1:n.*1143C=
ENST00000684667.1:c.1808C= ENSP00000507003.1:n.1808C=
ENST00000268097.10:c.1477C= MANE Select ENSP00000268097.6:p.Leu493=
ENST00000268097.9:c.1477C= ENSP00000268097.5:p.Leu493=
ENST00000379915.4:c.559C= ENSP00000478716.1:p.Leu187=
ENST00000564677.5:n.269C=
ENST00000565873.1:n.388C=
ENST00000566304.5:c.1510C= ENSP00000455114.1:p.Leu504=
ENST00000567027.5:c.1092C=
ENST00000567159.5:c.1477C= ENSP00000456489.1:p.Leu493=
ENST00000567411.5:c.*998C= ENSP00000455545.1:n.*998C=
ENST00000568777.5:n.6697C=
ENST00000569116.1:n.184C=
NM_000520.4:c.1477C= NP_000511.2:p.Leu493=
NM_000520.5:c.1477C= NP_000511.2:p.Leu493=
NM_001318825.1:c.1510C= NP_001305754.1:p.Leu504=
NR_134869.1:n.1721C=
NM_000520.6:c.1477C= MANE Select NP_000511.2:p.Leu493=
NM_001318825.2:c.1510C= NP_001305754.1:p.Leu504=
NR_134869.2:n.1262C=
NR_134869.3:n.1262C=