Canonical Allele Identifier: CA2186743006
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72344940T= , CM000677.2:g.72344940T= GRCh38
NC_000015.9:g.72637281T= , CM000677.1:g.72637281T= GRCh37
NC_000015.8:g.70424335T= NCBI36
NG_009017.1:g.36240A=
NG_009017.2:g.36240A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682064.1:n.1753+506A=
ENST00000682235.1:n.1549+506A=
ENST00000682461.1:c.1632+506A= ENSP00000507308.1:n.1632+506A=
ENST00000682653.1:n.3036A=
ENST00000682721.1:c.*1329+506A= ENSP00000507535.1:n.*1329+506A=
ENST00000682843.1:c.*1167+506A= ENSP00000508173.1:n.*1167+506A=
ENST00000683133.1:c.1710+506A= ENSP00000508108.1:n.1710+506A=
ENST00000683243.1:c.*679+506A= ENSP00000507042.1:n.*679+506A=
ENST00000683463.1:c.*1015+506A= ENSP00000507986.1:n.*1015+506A=
ENST00000683548.1:n.1984+506A=
ENST00000683579.1:c.*1424+506A= ENSP00000506867.1:n.*1424+506A=
ENST00000683587.1:n.2057+506A=
ENST00000683681.1:c.*204+506A= ENSP00000508110.1:n.*204+506A=
ENST00000683735.1:c.*1924+506A= ENSP00000508336.1:n.*1924+506A=
ENST00000683853.1:c.*837A= ENSP00000506834.1:n.*837A=
ENST00000683860.1:c.*646+506A= ENSP00000507179.1:n.*646+506A=
ENST00000684125.1:c.*186+506A= ENSP00000507320.1:n.*186+506A=
ENST00000684203.1:n.3975+506A=
ENST00000684231.1:c.*936+506A= ENSP00000507748.1:n.*936+506A=
ENST00000684263.1:c.*1150+506A= ENSP00000508369.1:n.*1150+506A=
ENST00000684305.1:c.1974+506A= ENSP00000506819.1:n.1974+506A=
ENST00000684602.1:c.*1192+506A= ENSP00000507996.1:n.*1192+506A=
ENST00000684667.1:c.1857+506A= ENSP00000507003.1:n.1857+506A=
ENST00000268097.10:c.1526+506A= MANE Select ENSP00000268097.6:n.1526+506A=
ENST00000268097.9:c.1526+506A= ENSP00000268097.5:n.1526+506A=
ENST00000379915.4:c.608+506A= ENSP00000478716.1:n.608+506A=
ENST00000564677.5:n.318+506A=
ENST00000565873.1:n.437+506A=
ENST00000566304.5:c.1559+506A= ENSP00000455114.1:n.1559+506A=
ENST00000567411.5:c.*1047+506A= ENSP00000455545.1:n.*1047+506A=
NM_000520.4:c.1526+506A= NP_000511.2:n.1526+506A=
NM_000520.5:c.1526+506A= NP_000511.2:n.1526+506A=
NM_001318825.1:c.1559+506A= NP_001305754.1:n.1559+506A=
NM_000520.6:c.1526+506A= MANE Select NP_000511.2:n.1526+506A=
NM_001318825.2:c.1559+506A= NP_001305754.1:n.1559+506A=