Canonical Allele Identifier: CA2186743351
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345687G= , CM000677.2:g.72345687G= GRCh38
NC_000015.9:g.72638028G= , CM000677.1:g.72638028G= GRCh37
NC_000015.8:g.70425082G= NCBI36
NG_009017.1:g.35493C=
NG_009017.2:g.35493C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*82-137C= ENSP00000457521.2:n.*82-137C=
ENST00000682061.1:c.*1631C= ENSP00000508316.1:n.*1631C=
ENST00000682064.1:n.1512C=
ENST00000682177.1:c.1465-137C= ENSP00000507409.1:n.1465-137C=
ENST00000682235.1:n.1308C=
ENST00000682461.1:c.1528-137C= ENSP00000507308.1:n.1528-137C=
ENST00000682653.1:n.2289C=
ENST00000682657.1:c.*1122C= ENSP00000507753.1:n.*1122C=
ENST00000682721.1:c.*1225-137C= ENSP00000507535.1:n.*1225-137C=
ENST00000682843.1:c.*1063-137C= ENSP00000508173.1:n.*1063-137C=
ENST00000683003.1:c.*1122C= ENSP00000507576.1:n.*1122C=
ENST00000683133.1:c.1606-137C= ENSP00000508108.1:n.1606-137C=
ENST00000683243.1:c.*575-137C= ENSP00000507042.1:n.*575-137C=
ENST00000683463.1:c.*774C= ENSP00000507986.1:n.*774C=
ENST00000683548.1:n.1743C=
ENST00000683579.1:c.*1320-137C= ENSP00000506867.1:n.*1320-137C=
ENST00000683587.1:n.1816C=
ENST00000683681.1:c.*89C= ENSP00000508110.1:n.*89C=
ENST00000683735.1:c.*1683C= ENSP00000508336.1:n.*1683C=
ENST00000683853.1:c.*227-137C= ENSP00000506834.1:n.*227-137C=
ENST00000683860.1:c.*405C= ENSP00000507179.1:n.*405C=
ENST00000683884.1:c.*612C= ENSP00000507004.1:n.*612C=
ENST00000684041.1:c.*544C= ENSP00000508382.1:n.*544C=
ENST00000684125.1:c.*82-137C= ENSP00000507320.1:n.*82-137C=
ENST00000684203.1:n.3734C=
ENST00000684231.1:c.*832-137C= ENSP00000507748.1:n.*832-137C=
ENST00000684263.1:c.*909C= ENSP00000508369.1:n.*909C=
ENST00000684305.1:c.1870-137C= ENSP00000506819.1:n.1870-137C=
ENST00000684415.1:c.*836C= ENSP00000507227.1:n.*836C=
ENST00000684520.1:c.*544C= ENSP00000506826.1:n.*544C=
ENST00000684602.1:c.*1088-137C= ENSP00000507996.1:n.*1088-137C=
ENST00000684667.1:c.1753-137C= ENSP00000507003.1:n.1753-137C=
ENST00000268097.10:c.1422-137C= MANE Select ENSP00000268097.6:n.1422-137C=
ENST00000268097.9:c.1422-137C= ENSP00000268097.5:n.1422-137C=
ENST00000379915.4:c.504-137C= ENSP00000478716.1:n.504-137C=
ENST00000564677.5:n.203C=
ENST00000565873.1:n.196C=
ENST00000566304.5:c.1455-137C= ENSP00000455114.1:n.1455-137C=
ENST00000567027.5:c.1037-137C=
ENST00000567159.5:c.1422-137C= ENSP00000456489.1:n.1422-137C=
ENST00000567411.5:c.*943-137C= ENSP00000455545.1:n.*943-137C=
ENST00000568777.5:n.6642-137C=
ENST00000569116.1:n.118C=
NM_000520.4:c.1422-137C= NP_000511.2:n.1422-137C=
NM_000520.5:c.1422-137C= NP_000511.2:n.1422-137C=
NM_001318825.1:c.1455-137C= NP_001305754.1:n.1455-137C=
NR_134869.1:n.1666-137C=
NM_000520.6:c.1422-137C= MANE Select NP_000511.2:n.1422-137C=
NM_001318825.2:c.1455-137C= NP_001305754.1:n.1455-137C=
NR_134869.2:n.1207-137C=
NR_134869.3:n.1207-137C=