Canonical Allele Identifier: CA2186743148
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345255G= , CM000677.2:g.72345255G= GRCh38
NC_000015.9:g.72637596G= , CM000677.1:g.72637596G= GRCh37
NC_000015.8:g.70424650G= NCBI36
NG_009017.1:g.35925C=
NG_009017.2:g.35925C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*377C= ENSP00000457521.2:n.*377C=
ENST00000682061.1:c.*2063C= ENSP00000508316.1:n.*2063C=
ENST00000682064.1:n.1753+191C=
ENST00000682235.1:n.1549+191C=
ENST00000682461.1:c.1632+191C= ENSP00000507308.1:n.1632+191C=
ENST00000682653.1:n.2721C=
ENST00000682657.1:c.*1554C= ENSP00000507753.1:n.*1554C=
ENST00000682721.1:c.*1329+191C= ENSP00000507535.1:n.*1329+191C=
ENST00000682843.1:c.*1167+191C= ENSP00000508173.1:n.*1167+191C=
ENST00000683133.1:c.1710+191C= ENSP00000508108.1:n.1710+191C=
ENST00000683243.1:c.*679+191C= ENSP00000507042.1:n.*679+191C=
ENST00000683463.1:c.*1015+191C= ENSP00000507986.1:n.*1015+191C=
ENST00000683548.1:n.1984+191C=
ENST00000683579.1:c.*1424+191C= ENSP00000506867.1:n.*1424+191C=
ENST00000683587.1:n.2057+191C=
ENST00000683681.1:c.*204+191C= ENSP00000508110.1:n.*204+191C=
ENST00000683735.1:c.*1924+191C= ENSP00000508336.1:n.*1924+191C=
ENST00000683853.1:c.*522C= ENSP00000506834.1:n.*522C=
ENST00000683860.1:c.*646+191C= ENSP00000507179.1:n.*646+191C=
ENST00000684125.1:c.*186+191C= ENSP00000507320.1:n.*186+191C=
ENST00000684203.1:n.3975+191C=
ENST00000684231.1:c.*936+191C= ENSP00000507748.1:n.*936+191C=
ENST00000684263.1:c.*1150+191C= ENSP00000508369.1:n.*1150+191C=
ENST00000684305.1:c.1974+191C= ENSP00000506819.1:n.1974+191C=
ENST00000684415.1:c.*1268C= ENSP00000507227.1:n.*1268C=
ENST00000684520.1:c.*976C= ENSP00000506826.1:n.*976C=
ENST00000684602.1:c.*1192+191C= ENSP00000507996.1:n.*1192+191C=
ENST00000684667.1:c.1857+191C= ENSP00000507003.1:n.1857+191C=
ENST00000268097.10:c.1526+191C= MANE Select ENSP00000268097.6:n.1526+191C=
ENST00000268097.9:c.1526+191C= ENSP00000268097.5:n.1526+191C=
ENST00000379915.4:c.608+191C= ENSP00000478716.1:n.608+191C=
ENST00000564677.5:n.318+191C=
ENST00000565873.1:n.437+191C=
ENST00000566304.5:c.1559+191C= ENSP00000455114.1:n.1559+191C=
ENST00000567027.5:c.1332C=
ENST00000567411.5:c.*1047+191C= ENSP00000455545.1:n.*1047+191C=
ENST00000569116.1:n.424C=
NM_000520.4:c.1526+191C= NP_000511.2:n.1526+191C=
NM_000520.5:c.1526+191C= NP_000511.2:n.1526+191C=
NM_001318825.1:c.1559+191C= NP_001305754.1:n.1559+191C=
NR_134869.1:n.1961C=
NM_000520.6:c.1526+191C= MANE Select NP_000511.2:n.1526+191C=
NM_001318825.2:c.1559+191C= NP_001305754.1:n.1559+191C=
NR_134869.2:n.1502C=
NR_134869.3:n.1502C=