Canonical Allele Identifier: CA2186744442
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72348110G= , CM000677.2:g.72348110G= GRCh38
NC_000015.9:g.72640451G= , CM000677.1:g.72640451G= GRCh37
NC_000015.8:g.70427505G= NCBI36
NG_009017.1:g.33070C=
NG_009017.2:g.33070C=

Transcript Alleles

HGVS Amino-acid change
ENST00000563908.2:n.3357C=
ENST00000567027.6:c.1011C= ENSP00000457521.2:p.Asp337=
ENST00000682061.1:c.*673C= ENSP00000508316.1:n.*673C=
ENST00000682177.1:c.1054C= ENSP00000507409.1:n.1054C=
ENST00000682461.1:c.1117C= ENSP00000507308.1:n.1117C=
ENST00000682653.1:n.1042C=
ENST00000682657.1:c.*421C= ENSP00000507753.1:n.*421C=
ENST00000682721.1:c.*814C= ENSP00000507535.1:n.*814C=
ENST00000682843.1:c.*909C= ENSP00000508173.1:n.*909C=
ENST00000683003.1:c.*421C= ENSP00000507576.1:n.*421C=
ENST00000683133.1:c.1195C= ENSP00000508108.1:n.1195C=
ENST00000683228.1:n.1042C=
ENST00000683243.1:c.*421C= ENSP00000507042.1:n.*421C=
ENST00000683463.1:c.1011C= ENSP00000507986.1:p.Asp337=
ENST00000683548.1:n.1042C=
ENST00000683579.1:c.*909C= ENSP00000506867.1:n.*909C=
ENST00000683587.1:n.1042C=
ENST00000683681.1:c.1011C= ENSP00000508110.1:p.Asp337=
ENST00000683735.1:c.*909C= ENSP00000508336.1:n.*909C=
ENST00000683742.1:n.842C=
ENST00000683853.1:c.1011C= ENSP00000506834.1:p.Asp337=
ENST00000683860.1:c.1011C= ENSP00000507179.1:p.Asp337=
ENST00000683884.1:c.1011C= ENSP00000507004.1:p.Asp337=
ENST00000684041.1:c.1011C= ENSP00000508382.1:p.Asp337=
ENST00000684125.1:c.1011C= ENSP00000507320.1:p.Asp337=
ENST00000684203.1:n.2849C=
ENST00000684231.1:c.*421C= ENSP00000507748.1:n.*421C=
ENST00000684263.1:c.1011C= ENSP00000508369.1:p.Asp337=
ENST00000684305.1:c.1459C= ENSP00000506819.1:n.1459C=
ENST00000684415.1:c.1011C= ENSP00000507227.1:p.Asp337=
ENST00000684520.1:c.1011C= ENSP00000506826.1:p.Asp337=
ENST00000684602.1:c.*677C= ENSP00000507996.1:n.*677C=
ENST00000684667.1:c.1342C= ENSP00000507003.1:n.1342C=
ENST00000268097.10:c.1011C= MANE Select ENSP00000268097.6:p.Asp337=
ENST00000268097.9:c.1011C= ENSP00000268097.5:p.Asp337=
ENST00000379915.4:c.413-1785C= ENSP00000478716.1:n.413-1785C=
ENST00000563762.5:c.763C= ENSP00000456346.1:n.763C=
ENST00000566304.5:c.1044C= ENSP00000455114.1:p.Asp348=
ENST00000566672.5:c.*421C= ENSP00000457037.1:n.*421C=
ENST00000567027.5:c.883C=
ENST00000567159.5:c.1011C= ENSP00000456489.1:p.Asp337=
ENST00000567411.5:c.*532C= ENSP00000455545.1:n.*532C=
ENST00000568777.5:n.6415C=
ENST00000569410.5:c.1011C= ENSP00000457125.1:p.Asp337=
NM_000520.4:c.1011C= NP_000511.2:p.Asp337=
NM_000520.5:c.1011C= NP_000511.2:p.Asp337=
NM_001318825.1:c.1044C= NP_001305754.1:p.Asp348=
NR_134869.1:n.1512C=
NM_000520.6:c.1011C= MANE Select NP_000511.2:p.Asp337=
NM_001318825.2:c.1044C= NP_001305754.1:p.Asp348=
NR_134869.2:n.1053C=
NR_134869.3:n.1053C=