Canonical Allele Identifier: CA2186743681
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72346577T= , CM000677.2:g.72346577T= GRCh38
NC_000015.9:g.72638918T= , CM000677.1:g.72638918T= GRCh37
NC_000015.8:g.70425972T= NCBI36
NG_009017.1:g.34603A=
NG_009017.2:g.34603A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.1074-252A= ENSP00000457521.2:n.1074-252A=
ENST00000682061.1:c.*942A= ENSP00000508316.1:n.*942A=
ENST00000682064.1:n.622A=
ENST00000682177.1:c.1323A= ENSP00000507409.1:n.1323A=
ENST00000682235.1:n.619A=
ENST00000682461.1:c.1386A= ENSP00000507308.1:n.1386A=
ENST00000682653.1:n.1600A=
ENST00000682657.1:c.*484-252A= ENSP00000507753.1:n.*484-252A=
ENST00000682721.1:c.*1083A= ENSP00000507535.1:n.*1083A=
ENST00000682843.1:c.*972-252A= ENSP00000508173.1:n.*972-252A=
ENST00000683003.1:c.*484-252A= ENSP00000507576.1:n.*484-252A=
ENST00000683133.1:c.1464A= ENSP00000508108.1:n.1464A=
ENST00000683243.1:c.*484-252A= ENSP00000507042.1:n.*484-252A=
ENST00000683463.1:c.*85A= ENSP00000507986.1:n.*85A=
ENST00000683548.1:n.1105-252A=
ENST00000683579.1:c.*1178A= ENSP00000506867.1:n.*1178A=
ENST00000683587.1:n.1178-252A=
ENST00000683681.1:c.1280A= ENSP00000508110.1:p.Tyr427=
ENST00000683735.1:c.*1045-252A= ENSP00000508336.1:n.*1045-252A=
ENST00000683853.1:c.*85A= ENSP00000506834.1:n.*85A=
ENST00000683860.1:c.1280A= ENSP00000507179.1:p.Tyr427=
ENST00000683884.1:c.1147-252A= ENSP00000507004.1:n.1147-252A=
ENST00000684041.1:c.1280A= ENSP00000508382.1:p.Tyr427=
ENST00000684125.1:c.1074-252A= ENSP00000507320.1:n.1074-252A=
ENST00000684203.1:n.3045A=
ENST00000684231.1:c.*690A= ENSP00000507748.1:n.*690A=
ENST00000684263.1:c.*220A= ENSP00000508369.1:n.*220A=
ENST00000684305.1:c.1728A= ENSP00000506819.1:n.1728A=
ENST00000684415.1:c.*147A= ENSP00000507227.1:n.*147A=
ENST00000684520.1:c.1280A= ENSP00000506826.1:p.Tyr427=
ENST00000684602.1:c.*946A= ENSP00000507996.1:n.*946A=
ENST00000684667.1:c.1611A= ENSP00000507003.1:n.1611A=
ENST00000268097.10:c.1280A= MANE Select ENSP00000268097.6:p.Tyr427=
ENST00000268097.9:c.1280A= ENSP00000268097.5:p.Tyr427=
ENST00000379915.4:c.413-252A= ENSP00000478716.1:n.413-252A=
ENST00000563762.5:c.826-252A= ENSP00000456346.1:n.826-252A=
ENST00000566304.5:c.1313A= ENSP00000455114.1:p.Tyr438=
ENST00000566672.5:c.*690A= ENSP00000457037.1:n.*690A=
ENST00000567027.5:c.946-252A=
ENST00000567159.5:c.1280A= ENSP00000456489.1:p.Tyr427=
ENST00000567411.5:c.*801A= ENSP00000455545.1:n.*801A=
ENST00000568777.5:n.6551-252A=
ENST00000569410.5:c.*85A= ENSP00000457125.1:n.*85A=
NM_000520.4:c.1280A= NP_000511.2:p.Tyr427=
NM_000520.5:c.1280A= NP_000511.2:p.Tyr427=
NM_001318825.1:c.1313A= NP_001305754.1:p.Tyr438=
NR_134869.1:n.1575-252A=
NM_000520.6:c.1280A= MANE Select NP_000511.2:p.Tyr427=
NM_001318825.2:c.1313A= NP_001305754.1:p.Tyr438=
NR_134869.2:n.1116-252A=
NR_134869.3:n.1116-252A=