Canonical Allele Identifier: CA2186743261
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345468G= , CM000677.2:g.72345468G= GRCh38
NC_000015.9:g.72637809G= , CM000677.1:g.72637809G= GRCh37
NC_000015.8:g.70424863G= NCBI36
NG_009017.1:g.35712C=
NG_009017.2:g.35712C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*164C= ENSP00000457521.2:n.*164C=
ENST00000682061.1:c.*1850C= ENSP00000508316.1:n.*1850C=
ENST00000682064.1:n.1731C=
ENST00000682177.1:c.1547C= ENSP00000507409.1:n.1547C=
ENST00000682235.1:n.1527C=
ENST00000682461.1:c.1610C= ENSP00000507308.1:n.1610C=
ENST00000682653.1:n.2508C=
ENST00000682657.1:c.*1341C= ENSP00000507753.1:n.*1341C=
ENST00000682721.1:c.*1307C= ENSP00000507535.1:n.*1307C=
ENST00000682843.1:c.*1145C= ENSP00000508173.1:n.*1145C=
ENST00000683003.1:c.*1341C= ENSP00000507576.1:n.*1341C=
ENST00000683133.1:c.1688C= ENSP00000508108.1:n.1688C=
ENST00000683243.1:c.*657C= ENSP00000507042.1:n.*657C=
ENST00000683463.1:c.*993C= ENSP00000507986.1:n.*993C=
ENST00000683548.1:n.1962C=
ENST00000683579.1:c.*1402C= ENSP00000506867.1:n.*1402C=
ENST00000683587.1:n.2035C=
ENST00000683681.1:c.*182C= ENSP00000508110.1:n.*182C=
ENST00000683735.1:c.*1902C= ENSP00000508336.1:n.*1902C=
ENST00000683853.1:c.*309C= ENSP00000506834.1:n.*309C=
ENST00000683860.1:c.*624C= ENSP00000507179.1:n.*624C=
ENST00000683884.1:c.*831C= ENSP00000507004.1:n.*831C=
ENST00000684041.1:c.*637C= ENSP00000508382.1:n.*637C=
ENST00000684125.1:c.*164C= ENSP00000507320.1:n.*164C=
ENST00000684203.1:n.3953C=
ENST00000684231.1:c.*914C= ENSP00000507748.1:n.*914C=
ENST00000684263.1:c.*1128C= ENSP00000508369.1:n.*1128C=
ENST00000684305.1:c.1952C= ENSP00000506819.1:n.1952C=
ENST00000684415.1:c.*1055C= ENSP00000507227.1:n.*1055C=
ENST00000684520.1:c.*763C= ENSP00000506826.1:n.*763C=
ENST00000684602.1:c.*1170C= ENSP00000507996.1:n.*1170C=
ENST00000684667.1:c.1835C= ENSP00000507003.1:n.1835C=
ENST00000268097.10:c.1504C= MANE Select ENSP00000268097.6:p.His502=
ENST00000268097.9:c.1504C= ENSP00000268097.5:p.His502=
ENST00000379915.4:c.586C= ENSP00000478716.1:p.His196=
ENST00000564677.5:n.296C=
ENST00000565873.1:n.415C=
ENST00000566304.5:c.1537C= ENSP00000455114.1:p.His513=
ENST00000567027.5:c.1119C=
ENST00000567159.5:c.1504C= ENSP00000456489.1:p.His502=
ENST00000567411.5:c.*1025C= ENSP00000455545.1:n.*1025C=
ENST00000568777.5:n.6724C=
ENST00000569116.1:n.211C=
NM_000520.4:c.1504C= NP_000511.2:p.His502=
NM_000520.5:c.1504C= NP_000511.2:p.His502=
NM_001318825.1:c.1537C= NP_001305754.1:p.His513=
NR_134869.1:n.1748C=
NM_000520.6:c.1504C= MANE Select NP_000511.2:p.His502=
NM_001318825.2:c.1537C= NP_001305754.1:p.His513=
NR_134869.2:n.1289C=
NR_134869.3:n.1289C=