Canonical Allele Identifier: CA2186743142
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345241A= , CM000677.2:g.72345241A= GRCh38
NC_000015.9:g.72637582A= , CM000677.1:g.72637582A= GRCh37
NC_000015.8:g.70424636A= NCBI36
NG_009017.1:g.35939T=
NG_009017.2:g.35939T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*391T= ENSP00000457521.2:n.*391T=
ENST00000682064.1:n.1753+205T=
ENST00000682235.1:n.1549+205T=
ENST00000682461.1:c.1632+205T= ENSP00000507308.1:n.1632+205T=
ENST00000682653.1:n.2735T=
ENST00000682721.1:c.*1329+205T= ENSP00000507535.1:n.*1329+205T=
ENST00000682843.1:c.*1167+205T= ENSP00000508173.1:n.*1167+205T=
ENST00000683133.1:c.1710+205T= ENSP00000508108.1:n.1710+205T=
ENST00000683243.1:c.*679+205T= ENSP00000507042.1:n.*679+205T=
ENST00000683463.1:c.*1015+205T= ENSP00000507986.1:n.*1015+205T=
ENST00000683548.1:n.1984+205T=
ENST00000683579.1:c.*1424+205T= ENSP00000506867.1:n.*1424+205T=
ENST00000683587.1:n.2057+205T=
ENST00000683681.1:c.*204+205T= ENSP00000508110.1:n.*204+205T=
ENST00000683735.1:c.*1924+205T= ENSP00000508336.1:n.*1924+205T=
ENST00000683853.1:c.*536T= ENSP00000506834.1:n.*536T=
ENST00000683860.1:c.*646+205T= ENSP00000507179.1:n.*646+205T=
ENST00000684125.1:c.*186+205T= ENSP00000507320.1:n.*186+205T=
ENST00000684203.1:n.3975+205T=
ENST00000684231.1:c.*936+205T= ENSP00000507748.1:n.*936+205T=
ENST00000684263.1:c.*1150+205T= ENSP00000508369.1:n.*1150+205T=
ENST00000684305.1:c.1974+205T= ENSP00000506819.1:n.1974+205T=
ENST00000684415.1:c.*1282T= ENSP00000507227.1:n.*1282T=
ENST00000684602.1:c.*1192+205T= ENSP00000507996.1:n.*1192+205T=
ENST00000684667.1:c.1857+205T= ENSP00000507003.1:n.1857+205T=
ENST00000268097.10:c.1526+205T= MANE Select ENSP00000268097.6:n.1526+205T=
ENST00000268097.9:c.1526+205T= ENSP00000268097.5:n.1526+205T=
ENST00000379915.4:c.608+205T= ENSP00000478716.1:n.608+205T=
ENST00000564677.5:n.318+205T=
ENST00000565873.1:n.437+205T=
ENST00000566304.5:c.1559+205T= ENSP00000455114.1:n.1559+205T=
ENST00000567027.5:c.1346T=
ENST00000567411.5:c.*1047+205T= ENSP00000455545.1:n.*1047+205T=
ENST00000569116.1:n.438T=
NM_000520.4:c.1526+205T= NP_000511.2:n.1526+205T=
NM_000520.5:c.1526+205T= NP_000511.2:n.1526+205T=
NM_001318825.1:c.1559+205T= NP_001305754.1:n.1559+205T=
NR_134869.1:n.1975T=
NM_000520.6:c.1526+205T= MANE Select NP_000511.2:n.1526+205T=
NM_001318825.2:c.1559+205T= NP_001305754.1:n.1559+205T=
NR_134869.2:n.1516T=
NR_134869.3:n.1516T=