Canonical Allele Identifier: CA2186743403
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345837A= , CM000677.2:g.72345837A= GRCh38
NC_000015.9:g.72638178A= , CM000677.1:g.72638178A= GRCh37
NC_000015.8:g.70425232A= NCBI36
NG_009017.1:g.35343T=
NG_009017.2:g.35343T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*82-287T= ENSP00000457521.2:n.*82-287T=
ENST00000682061.1:c.*1481T= ENSP00000508316.1:n.*1481T=
ENST00000682064.1:n.1362T=
ENST00000682177.1:c.1465-287T= ENSP00000507409.1:n.1465-287T=
ENST00000682235.1:n.1158T=
ENST00000682461.1:c.1528-287T= ENSP00000507308.1:n.1528-287T=
ENST00000682653.1:n.2139T=
ENST00000682657.1:c.*972T= ENSP00000507753.1:n.*972T=
ENST00000682721.1:c.*1225-287T= ENSP00000507535.1:n.*1225-287T=
ENST00000682843.1:c.*1063-287T= ENSP00000508173.1:n.*1063-287T=
ENST00000683003.1:c.*972T= ENSP00000507576.1:n.*972T=
ENST00000683133.1:c.1606-287T= ENSP00000508108.1:n.1606-287T=
ENST00000683243.1:c.*575-287T= ENSP00000507042.1:n.*575-287T=
ENST00000683463.1:c.*624T= ENSP00000507986.1:n.*624T=
ENST00000683548.1:n.1593T=
ENST00000683579.1:c.*1320-287T= ENSP00000506867.1:n.*1320-287T=
ENST00000683587.1:n.1666T=
ENST00000683681.1:c.1422-61T= ENSP00000508110.1:n.1422-61T=
ENST00000683735.1:c.*1533T= ENSP00000508336.1:n.*1533T=
ENST00000683853.1:c.*227-287T= ENSP00000506834.1:n.*227-287T=
ENST00000683860.1:c.*255T= ENSP00000507179.1:n.*255T=
ENST00000683884.1:c.*462T= ENSP00000507004.1:n.*462T=
ENST00000684041.1:c.*394T= ENSP00000508382.1:n.*394T=
ENST00000684125.1:c.*82-287T= ENSP00000507320.1:n.*82-287T=
ENST00000684203.1:n.3584T=
ENST00000684231.1:c.*832-287T= ENSP00000507748.1:n.*832-287T=
ENST00000684263.1:c.*759T= ENSP00000508369.1:n.*759T=
ENST00000684305.1:c.1870-287T= ENSP00000506819.1:n.1870-287T=
ENST00000684415.1:c.*686T= ENSP00000507227.1:n.*686T=
ENST00000684520.1:c.*394T= ENSP00000506826.1:n.*394T=
ENST00000684602.1:c.*1088-287T= ENSP00000507996.1:n.*1088-287T=
ENST00000684667.1:c.1753-287T= ENSP00000507003.1:n.1753-287T=
ENST00000268097.10:c.1422-287T= MANE Select ENSP00000268097.6:n.1422-287T=
ENST00000268097.9:c.1422-287T= ENSP00000268097.5:n.1422-287T=
ENST00000379915.4:c.504-287T= ENSP00000478716.1:n.504-287T=
ENST00000564677.5:n.53T=
ENST00000565873.1:n.46T=
ENST00000566304.5:c.1455-287T= ENSP00000455114.1:n.1455-287T=
ENST00000567027.5:c.1037-287T=
ENST00000567159.5:c.1422-287T= ENSP00000456489.1:n.1422-287T=
ENST00000567411.5:c.*943-287T= ENSP00000455545.1:n.*943-287T=
ENST00000568777.5:n.6642-287T=
NM_000520.4:c.1422-287T= NP_000511.2:n.1422-287T=
NM_000520.5:c.1422-287T= NP_000511.2:n.1422-287T=
NM_001318825.1:c.1455-287T= NP_001305754.1:n.1455-287T=
NR_134869.1:n.1666-287T=
NM_000520.6:c.1422-287T= MANE Select NP_000511.2:n.1422-287T=
NM_001318825.2:c.1455-287T= NP_001305754.1:n.1455-287T=
NR_134869.2:n.1207-287T=
NR_134869.3:n.1207-287T=