Canonical Allele Identifier: CA2186743572
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346305G= , CM000677.2:g.72346305G= GRCh38
NC_000015.9:g.72638646G= , CM000677.1:g.72638646G= GRCh37
NC_000015.8:g.70425700G= NCBI36
NG_009017.1:g.34875C=
NG_009017.2:g.34875C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*11C= ENSP00000457521.2:n.*11C=
ENST00000682061.1:c.*1013C= ENSP00000508316.1:n.*1013C=
ENST00000682064.1:n.894C=
ENST00000682177.1:c.1394C= ENSP00000507409.1:n.1394C=
ENST00000682235.1:n.690C=
ENST00000682461.1:c.1457C= ENSP00000507308.1:n.1457C=
ENST00000682653.1:n.1671C=
ENST00000682657.1:c.*504C= ENSP00000507753.1:n.*504C=
ENST00000682721.1:c.*1154C= ENSP00000507535.1:n.*1154C=
ENST00000682843.1:c.*992C= ENSP00000508173.1:n.*992C=
ENST00000683003.1:c.*504C= ENSP00000507576.1:n.*504C=
ENST00000683133.1:c.1535C= ENSP00000508108.1:n.1535C=
ENST00000683243.1:c.*504C= ENSP00000507042.1:n.*504C=
ENST00000683463.1:c.*156C= ENSP00000507986.1:n.*156C=
ENST00000683548.1:n.1125C=
ENST00000683579.1:c.*1249C= ENSP00000506867.1:n.*1249C=
ENST00000683587.1:n.1198C=
ENST00000683681.1:c.1351C= ENSP00000508110.1:p.Leu451=
ENST00000683735.1:c.*1065C= ENSP00000508336.1:n.*1065C=
ENST00000683853.1:c.*156C= ENSP00000506834.1:n.*156C=
ENST00000683860.1:c.1351C= ENSP00000507179.1:p.Leu451=
ENST00000683884.1:c.1167C= ENSP00000507004.1:p.Leu389=
ENST00000684041.1:c.1351C= ENSP00000508382.1:p.Leu451=
ENST00000684125.1:c.*11C= ENSP00000507320.1:n.*11C=
ENST00000684203.1:n.3116C=
ENST00000684231.1:c.*761C= ENSP00000507748.1:n.*761C=
ENST00000684263.1:c.*291C= ENSP00000508369.1:n.*291C=
ENST00000684305.1:c.1799C= ENSP00000506819.1:n.1799C=
ENST00000684415.1:c.*218C= ENSP00000507227.1:n.*218C=
ENST00000684520.1:c.1351C= ENSP00000506826.1:p.Leu451=
ENST00000684602.1:c.*1017C= ENSP00000507996.1:n.*1017C=
ENST00000684667.1:c.1682C= ENSP00000507003.1:n.1682C=
ENST00000268097.10:c.1351C= MANE Select ENSP00000268097.6:p.Leu451=
ENST00000268097.9:c.1351C= ENSP00000268097.5:p.Leu451=
ENST00000379915.4:c.433C= ENSP00000478716.1:p.Leu145=
ENST00000563762.5:c.846C= ENSP00000456346.1:n.846C=
ENST00000566304.5:c.1384C= ENSP00000455114.1:p.Leu462=
ENST00000566672.5:c.*761C= ENSP00000457037.1:n.*761C=
ENST00000567027.5:c.966C=
ENST00000567159.5:c.1351C= ENSP00000456489.1:p.Leu451=
ENST00000567411.5:c.*872C= ENSP00000455545.1:n.*872C=
ENST00000568777.5:n.6571C=
ENST00000569410.5:c.*156C= ENSP00000457125.1:n.*156C=
NM_000520.4:c.1351C= NP_000511.2:p.Leu451=
NM_000520.5:c.1351C= NP_000511.2:p.Leu451=
NM_001318825.1:c.1384C= NP_001305754.1:p.Leu462=
NR_134869.1:n.1595C=
NM_000520.6:c.1351C= MANE Select NP_000511.2:p.Leu451=
NM_001318825.2:c.1384C= NP_001305754.1:p.Leu462=
NR_134869.2:n.1136C=
NR_134869.3:n.1136C=