Canonical Allele Identifier: CA2186743556
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346269A= , CM000677.2:g.72346269A= GRCh38
NC_000015.9:g.72638610A= , CM000677.1:g.72638610A= GRCh37
NC_000015.8:g.70425664A= NCBI36
NG_009017.1:g.34911T=
NG_009017.2:g.34911T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*47T= ENSP00000457521.2:n.*47T=
ENST00000682061.1:c.*1049T= ENSP00000508316.1:n.*1049T=
ENST00000682064.1:n.930T=
ENST00000682177.1:c.1430T= ENSP00000507409.1:n.1430T=
ENST00000682235.1:n.726T=
ENST00000682461.1:c.1493T= ENSP00000507308.1:n.1493T=
ENST00000682653.1:n.1707T=
ENST00000682657.1:c.*540T= ENSP00000507753.1:n.*540T=
ENST00000682721.1:c.*1190T= ENSP00000507535.1:n.*1190T=
ENST00000682843.1:c.*1028T= ENSP00000508173.1:n.*1028T=
ENST00000683003.1:c.*540T= ENSP00000507576.1:n.*540T=
ENST00000683133.1:c.1571T= ENSP00000508108.1:n.1571T=
ENST00000683243.1:c.*540T= ENSP00000507042.1:n.*540T=
ENST00000683463.1:c.*192T= ENSP00000507986.1:n.*192T=
ENST00000683548.1:n.1161T=
ENST00000683579.1:c.*1285T= ENSP00000506867.1:n.*1285T=
ENST00000683587.1:n.1234T=
ENST00000683681.1:c.1387T= ENSP00000508110.1:p.Tyr463=
ENST00000683735.1:c.*1101T= ENSP00000508336.1:n.*1101T=
ENST00000683853.1:c.*192T= ENSP00000506834.1:n.*192T=
ENST00000683860.1:c.1387T= ENSP00000507179.1:p.Tyr463=
ENST00000683884.1:c.*30T= ENSP00000507004.1:n.*30T=
ENST00000684041.1:c.1387T= ENSP00000508382.1:p.Tyr463=
ENST00000684125.1:c.*47T= ENSP00000507320.1:n.*47T=
ENST00000684203.1:n.3152T=
ENST00000684231.1:c.*797T= ENSP00000507748.1:n.*797T=
ENST00000684263.1:c.*327T= ENSP00000508369.1:n.*327T=
ENST00000684305.1:c.1835T= ENSP00000506819.1:n.1835T=
ENST00000684415.1:c.*254T= ENSP00000507227.1:n.*254T=
ENST00000684520.1:c.1387T= ENSP00000506826.1:p.Tyr463=
ENST00000684602.1:c.*1053T= ENSP00000507996.1:n.*1053T=
ENST00000684667.1:c.1718T= ENSP00000507003.1:n.1718T=
ENST00000268097.10:c.1387T= MANE Select ENSP00000268097.6:p.Tyr463=
ENST00000268097.9:c.1387T= ENSP00000268097.5:p.Tyr463=
ENST00000379915.4:c.469T= ENSP00000478716.1:p.Tyr157=
ENST00000563762.5:c.882T= ENSP00000456346.1:n.882T=
ENST00000566304.5:c.1420T= ENSP00000455114.1:p.Tyr474=
ENST00000566672.5:c.*797T= ENSP00000457037.1:n.*797T=
ENST00000567027.5:c.1002T=
ENST00000567159.5:c.1387T= ENSP00000456489.1:p.Tyr463=
ENST00000567411.5:c.*908T= ENSP00000455545.1:n.*908T=
ENST00000568777.5:n.6607T=
ENST00000569410.5:c.*192T= ENSP00000457125.1:n.*192T=
NM_000520.4:c.1387T= NP_000511.2:p.Tyr463=
NM_000520.5:c.1387T= NP_000511.2:p.Tyr463=
NM_001318825.1:c.1420T= NP_001305754.1:p.Tyr474=
NR_134869.1:n.1631T=
NM_000520.6:c.1387T= MANE Select NP_000511.2:p.Tyr463=
NM_001318825.2:c.1420T= NP_001305754.1:p.Tyr474=
NR_134869.2:n.1172T=
NR_134869.3:n.1172T=