Canonical Allele Identifier: CA16044211
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72353727del , CM000677.2:g.72353727del GRCh38
NC_000015.9:g.72646068del , CM000677.1:g.72646068del GRCh37
NC_000015.8:g.70433122del NCBI36
NG_009017.1:g.27456del
NG_009017.2:g.27456del

Transcript Alleles

HGVS Amino-acid Change
ENST00000563908.2:n.2260del
ENST00000567027.6:c.426del ENSP00000457521.2:p.Phe142LeufsTer?
ENST00000568260.2:c.480-546del ENSP00000458128.2:n.480-546del
ENST00000682061.1:c.*88del ENSP00000508316.1:n.*88del
ENST00000682177.1:c.426del ENSP00000507409.1:p.Phe142LeufsTer?
ENST00000682461.1:c.676+1835del ENSP00000507308.1:n.676+1835del
ENST00000682653.1:n.457del
ENST00000682657.1:c.254-2490del ENSP00000507753.1:n.254-2490del
ENST00000682721.1:c.*229del ENSP00000507535.1:n.*229del
ENST00000682843.1:c.*324del ENSP00000508173.1:n.*324del
ENST00000683003.1:c.412+1835del ENSP00000507576.1:n.412+1835del
ENST00000683133.1:c.610del ENSP00000508108.1:n.610del
ENST00000683228.1:n.457del
ENST00000683243.1:c.412+1835del ENSP00000507042.1:n.412+1835del
ENST00000683463.1:c.426del ENSP00000507986.1:p.Phe142LeufsTer?
ENST00000683548.1:n.457del
ENST00000683579.1:c.*324del ENSP00000506867.1:n.*324del
ENST00000683587.1:n.457del
ENST00000683681.1:c.426del ENSP00000508110.1:p.Phe142LeufsTer?
ENST00000683735.1:c.*324del ENSP00000508336.1:n.*324del
ENST00000683853.1:c.426del ENSP00000506834.1:p.Phe142LeufsTer?
ENST00000683860.1:c.426del ENSP00000507179.1:p.Phe142LeufsTer?
ENST00000683884.1:c.426del ENSP00000507004.1:p.Phe142LeufsTer?
ENST00000684041.1:c.426del ENSP00000508382.1:p.Phe142LeufsTer?
ENST00000684125.1:c.426del ENSP00000507320.1:p.Phe142LeufsTer?
ENST00000684203.1:n.2264del
ENST00000684231.1:c.412+1835del ENSP00000507748.1:n.412+1835del
ENST00000684263.1:c.426del ENSP00000508369.1:p.Phe142LeufsTer?
ENST00000684305.1:c.874del ENSP00000506819.1:n.874del
ENST00000684415.1:c.426del ENSP00000507227.1:p.Phe142LeufsTer?
ENST00000684520.1:c.426del ENSP00000506826.1:p.Phe142LeufsTer?
ENST00000684602.1:c.*236+1835del ENSP00000507996.1:n.*236+1835del
ENST00000684667.1:c.757del ENSP00000507003.1:n.757del
ENST00000268097.10:c.426del MANE Select ENSP00000268097.6:p.Phe142LeufsTer?
ENST00000268097.9:c.426del ENSP00000268097.5:p.Phe142LeufsTer?
ENST00000379915.4:c.412+1835del ENSP00000478716.1:n.412+1835del
ENST00000563762.5:c.503+1835del ENSP00000456346.1:n.503+1835del
ENST00000566304.5:c.459del ENSP00000455114.1:p.Phe153LeufsTer?
ENST00000566672.5:c.412+1835del ENSP00000457037.1:n.412+1835del
ENST00000567027.5:c.298del
ENST00000567159.5:c.426del ENSP00000456489.1:p.Phe142LeufsTer?
ENST00000567411.5:c.413-546del ENSP00000455545.1:n.413-546del
ENST00000568260.1:c.461-546del
ENST00000568777.5:n.5830del
ENST00000569410.5:c.426del ENSP00000457125.1:p.Phe142LeufsTer?
ENST00000569509.5:n.417+1835del
NM_000520.4:c.426del NP_000511.2:p.Phe142LeufsTer?
NM_000520.5:c.426del NP_000511.2:p.Phe142LeufsTer?
NM_001318825.1:c.459del NP_001305754.1:p.Phe153LeufsTer?
NR_134869.1:n.927del
NM_000520.6:c.426del MANE Select NP_000511.2:p.Phe142LeufsTer?
NM_001318825.2:c.459del NP_001305754.1:p.Phe153LeufsTer?
NR_134869.2:n.468del
NR_134869.3:n.468del