Canonical Allele Identifier: CA2186743064
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345070G= , CM000677.2:g.72345070G= GRCh38
NC_000015.9:g.72637411G= , CM000677.1:g.72637411G= GRCh37
NC_000015.8:g.70424465G= NCBI36
NG_009017.1:g.36110C=
NG_009017.2:g.36110C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682064.1:n.1753+376C=
ENST00000682235.1:n.1549+376C=
ENST00000682461.1:c.1632+376C= ENSP00000507308.1:n.1632+376C=
ENST00000682653.1:n.2906C=
ENST00000682721.1:c.*1329+376C= ENSP00000507535.1:n.*1329+376C=
ENST00000682843.1:c.*1167+376C= ENSP00000508173.1:n.*1167+376C=
ENST00000683133.1:c.1710+376C= ENSP00000508108.1:n.1710+376C=
ENST00000683243.1:c.*679+376C= ENSP00000507042.1:n.*679+376C=
ENST00000683463.1:c.*1015+376C= ENSP00000507986.1:n.*1015+376C=
ENST00000683548.1:n.1984+376C=
ENST00000683579.1:c.*1424+376C= ENSP00000506867.1:n.*1424+376C=
ENST00000683587.1:n.2057+376C=
ENST00000683681.1:c.*204+376C= ENSP00000508110.1:n.*204+376C=
ENST00000683735.1:c.*1924+376C= ENSP00000508336.1:n.*1924+376C=
ENST00000683853.1:c.*707C= ENSP00000506834.1:n.*707C=
ENST00000683860.1:c.*646+376C= ENSP00000507179.1:n.*646+376C=
ENST00000684125.1:c.*186+376C= ENSP00000507320.1:n.*186+376C=
ENST00000684203.1:n.3975+376C=
ENST00000684231.1:c.*936+376C= ENSP00000507748.1:n.*936+376C=
ENST00000684263.1:c.*1150+376C= ENSP00000508369.1:n.*1150+376C=
ENST00000684305.1:c.1974+376C= ENSP00000506819.1:n.1974+376C=
ENST00000684602.1:c.*1192+376C= ENSP00000507996.1:n.*1192+376C=
ENST00000684667.1:c.1857+376C= ENSP00000507003.1:n.1857+376C=
ENST00000268097.10:c.1526+376C= MANE Select ENSP00000268097.6:n.1526+376C=
ENST00000268097.9:c.1526+376C= ENSP00000268097.5:n.1526+376C=
ENST00000379915.4:c.608+376C= ENSP00000478716.1:n.608+376C=
ENST00000564677.5:n.318+376C=
ENST00000565873.1:n.437+376C=
ENST00000566304.5:c.1559+376C= ENSP00000455114.1:n.1559+376C=
ENST00000567411.5:c.*1047+376C= ENSP00000455545.1:n.*1047+376C=
NM_000520.4:c.1526+376C= NP_000511.2:n.1526+376C=
NM_000520.5:c.1526+376C= NP_000511.2:n.1526+376C=
NM_001318825.1:c.1559+376C= NP_001305754.1:n.1559+376C=
NM_000520.6:c.1526+376C= MANE Select NP_000511.2:n.1526+376C=
NM_001318825.2:c.1559+376C= NP_001305754.1:n.1559+376C=