Canonical Allele Identifier: CA2186743007
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72344947G= , CM000677.2:g.72344947G= GRCh38
NC_000015.9:g.72637288G= , CM000677.1:g.72637288G= GRCh37
NC_000015.8:g.70424342G= NCBI36
NG_009017.1:g.36233C=
NG_009017.2:g.36233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682064.1:n.1753+499C=
ENST00000682235.1:n.1549+499C=
ENST00000682461.1:c.1632+499C= ENSP00000507308.1:n.1632+499C=
ENST00000682653.1:n.3029C=
ENST00000682721.1:c.*1329+499C= ENSP00000507535.1:n.*1329+499C=
ENST00000682843.1:c.*1167+499C= ENSP00000508173.1:n.*1167+499C=
ENST00000683133.1:c.1710+499C= ENSP00000508108.1:n.1710+499C=
ENST00000683243.1:c.*679+499C= ENSP00000507042.1:n.*679+499C=
ENST00000683463.1:c.*1015+499C= ENSP00000507986.1:n.*1015+499C=
ENST00000683548.1:n.1984+499C=
ENST00000683579.1:c.*1424+499C= ENSP00000506867.1:n.*1424+499C=
ENST00000683587.1:n.2057+499C=
ENST00000683681.1:c.*204+499C= ENSP00000508110.1:n.*204+499C=
ENST00000683735.1:c.*1924+499C= ENSP00000508336.1:n.*1924+499C=
ENST00000683853.1:c.*830C= ENSP00000506834.1:n.*830C=
ENST00000683860.1:c.*646+499C= ENSP00000507179.1:n.*646+499C=
ENST00000684125.1:c.*186+499C= ENSP00000507320.1:n.*186+499C=
ENST00000684203.1:n.3975+499C=
ENST00000684231.1:c.*936+499C= ENSP00000507748.1:n.*936+499C=
ENST00000684263.1:c.*1150+499C= ENSP00000508369.1:n.*1150+499C=
ENST00000684305.1:c.1974+499C= ENSP00000506819.1:n.1974+499C=
ENST00000684602.1:c.*1192+499C= ENSP00000507996.1:n.*1192+499C=
ENST00000684667.1:c.1857+499C= ENSP00000507003.1:n.1857+499C=
ENST00000268097.10:c.1526+499C= MANE Select ENSP00000268097.6:n.1526+499C=
ENST00000268097.9:c.1526+499C= ENSP00000268097.5:n.1526+499C=
ENST00000379915.4:c.608+499C= ENSP00000478716.1:n.608+499C=
ENST00000564677.5:n.318+499C=
ENST00000565873.1:n.437+499C=
ENST00000566304.5:c.1559+499C= ENSP00000455114.1:n.1559+499C=
ENST00000567411.5:c.*1047+499C= ENSP00000455545.1:n.*1047+499C=
NM_000520.4:c.1526+499C= NP_000511.2:n.1526+499C=
NM_000520.5:c.1526+499C= NP_000511.2:n.1526+499C=
NM_001318825.1:c.1559+499C= NP_001305754.1:n.1559+499C=
NM_000520.6:c.1526+499C= MANE Select NP_000511.2:n.1526+499C=
NM_001318825.2:c.1559+499C= NP_001305754.1:n.1559+499C=