Canonical Allele Identifier: CA2186743413
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345876A= , CM000677.2:g.72345876A= GRCh38
NC_000015.9:g.72638217A= , CM000677.1:g.72638217A= GRCh37
NC_000015.8:g.70425271A= NCBI36
NG_009017.1:g.35304T=
NG_009017.2:g.35304T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*82-326T= ENSP00000457521.2:n.*82-326T=
ENST00000682061.1:c.*1442T= ENSP00000508316.1:n.*1442T=
ENST00000682064.1:n.1323T=
ENST00000682177.1:c.1465-326T= ENSP00000507409.1:n.1465-326T=
ENST00000682235.1:n.1119T=
ENST00000682461.1:c.1528-326T= ENSP00000507308.1:n.1528-326T=
ENST00000682653.1:n.2100T=
ENST00000682657.1:c.*933T= ENSP00000507753.1:n.*933T=
ENST00000682721.1:c.*1225-326T= ENSP00000507535.1:n.*1225-326T=
ENST00000682843.1:c.*1063-326T= ENSP00000508173.1:n.*1063-326T=
ENST00000683003.1:c.*933T= ENSP00000507576.1:n.*933T=
ENST00000683133.1:c.1606-326T= ENSP00000508108.1:n.1606-326T=
ENST00000683243.1:c.*575-326T= ENSP00000507042.1:n.*575-326T=
ENST00000683463.1:c.*585T= ENSP00000507986.1:n.*585T=
ENST00000683548.1:n.1554T=
ENST00000683579.1:c.*1320-326T= ENSP00000506867.1:n.*1320-326T=
ENST00000683587.1:n.1627T=
ENST00000683681.1:c.1422-100T= ENSP00000508110.1:n.1422-100T=
ENST00000683735.1:c.*1494T= ENSP00000508336.1:n.*1494T=
ENST00000683853.1:c.*227-326T= ENSP00000506834.1:n.*227-326T=
ENST00000683860.1:c.*216T= ENSP00000507179.1:n.*216T=
ENST00000683884.1:c.*423T= ENSP00000507004.1:n.*423T=
ENST00000684041.1:c.*355T= ENSP00000508382.1:n.*355T=
ENST00000684125.1:c.*82-326T= ENSP00000507320.1:n.*82-326T=
ENST00000684203.1:n.3545T=
ENST00000684231.1:c.*832-326T= ENSP00000507748.1:n.*832-326T=
ENST00000684263.1:c.*720T= ENSP00000508369.1:n.*720T=
ENST00000684305.1:c.1870-326T= ENSP00000506819.1:n.1870-326T=
ENST00000684415.1:c.*647T= ENSP00000507227.1:n.*647T=
ENST00000684520.1:c.*355T= ENSP00000506826.1:n.*355T=
ENST00000684602.1:c.*1088-326T= ENSP00000507996.1:n.*1088-326T=
ENST00000684667.1:c.1753-326T= ENSP00000507003.1:n.1753-326T=
ENST00000268097.10:c.1422-326T= MANE Select ENSP00000268097.6:n.1422-326T=
ENST00000268097.9:c.1422-326T= ENSP00000268097.5:n.1422-326T=
ENST00000379915.4:c.504-326T= ENSP00000478716.1:n.504-326T=
ENST00000564677.5:n.14T=
ENST00000565873.1:n.7T=
ENST00000566304.5:c.1455-326T= ENSP00000455114.1:n.1455-326T=
ENST00000567027.5:c.1037-326T=
ENST00000567159.5:c.1422-326T= ENSP00000456489.1:n.1422-326T=
ENST00000567411.5:c.*943-326T= ENSP00000455545.1:n.*943-326T=
ENST00000568777.5:n.6642-326T=
NM_000520.4:c.1422-326T= NP_000511.2:n.1422-326T=
NM_000520.5:c.1422-326T= NP_000511.2:n.1422-326T=
NM_001318825.1:c.1455-326T= NP_001305754.1:n.1455-326T=
NR_134869.1:n.1666-326T=
NM_000520.6:c.1422-326T= MANE Select NP_000511.2:n.1422-326T=
NM_001318825.2:c.1455-326T= NP_001305754.1:n.1455-326T=
NR_134869.2:n.1207-326T=
NR_134869.3:n.1207-326T=