Canonical Allele Identifier: CA2186747536
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72355601G= , CM000677.2:g.72355601G= GRCh38
NC_000015.9:g.72647942G= , CM000677.1:g.72647942G= GRCh37
NC_000015.8:g.70434996G= NCBI36
NG_009017.1:g.25579C=
NG_009017.2:g.25579C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000563908.2:n.383C=
ENST00000567027.6:c.370C= ENSP00000457521.2:p.Gln124=
ENST00000568260.2:c.437C= ENSP00000458128.2:n.437C=
ENST00000682061.1:c.*32C= ENSP00000508316.1:n.*32C=
ENST00000682177.1:c.370C= ENSP00000507409.1:p.Gln124=
ENST00000682461.1:c.634C= ENSP00000507308.1:n.634C=
ENST00000682653.1:n.401C=
ENST00000682657.1:c.254-4367C= ENSP00000507753.1:n.254-4367C=
ENST00000682721.1:c.*173C= ENSP00000507535.1:n.*173C=
ENST00000682843.1:c.*268C= ENSP00000508173.1:n.*268C=
ENST00000683003.1:c.370C= ENSP00000507576.1:p.Gln124=
ENST00000683133.1:c.554C= ENSP00000508108.1:n.554C=
ENST00000683228.1:n.401C=
ENST00000683243.1:c.370C= ENSP00000507042.1:p.Gln124=
ENST00000683463.1:c.370C= ENSP00000507986.1:p.Gln124=
ENST00000683548.1:n.401C=
ENST00000683579.1:c.*268C= ENSP00000506867.1:n.*268C=
ENST00000683587.1:n.401C=
ENST00000683681.1:c.370C= ENSP00000508110.1:p.Gln124=
ENST00000683735.1:c.*268C= ENSP00000508336.1:n.*268C=
ENST00000683853.1:c.370C= ENSP00000506834.1:p.Gln124=
ENST00000683860.1:c.370C= ENSP00000507179.1:p.Gln124=
ENST00000683884.1:c.370C= ENSP00000507004.1:p.Gln124=
ENST00000684041.1:c.370C= ENSP00000508382.1:p.Gln124=
ENST00000684125.1:c.370C= ENSP00000507320.1:p.Gln124=
ENST00000684203.1:n.387C=
ENST00000684231.1:c.370C= ENSP00000507748.1:p.Gln124=
ENST00000684263.1:c.370C= ENSP00000508369.1:p.Gln124=
ENST00000684305.1:c.818C= ENSP00000506819.1:n.818C=
ENST00000684415.1:c.370C= ENSP00000507227.1:p.Gln124=
ENST00000684520.1:c.370C= ENSP00000506826.1:p.Gln124=
ENST00000684602.1:c.*194C= ENSP00000507996.1:n.*194C=
ENST00000684667.1:c.701C= ENSP00000507003.1:n.701C=
ENST00000268097.10:c.370C= MANE Select ENSP00000268097.6:p.Gln124=
ENST00000268097.9:c.370C= ENSP00000268097.5:p.Gln124=
ENST00000379915.4:c.370C= ENSP00000478716.1:p.Gln124=
ENST00000563762.5:c.461C= ENSP00000456346.1:n.461C=
ENST00000563908.1:n.367C=
ENST00000566304.5:c.403C= ENSP00000455114.1:p.Gln135=
ENST00000566672.5:c.370C= ENSP00000457037.1:p.Gln124=
ENST00000567027.5:c.242C=
ENST00000567159.5:c.370C= ENSP00000456489.1:p.Gln124=
ENST00000567411.5:c.370C= ENSP00000455545.1:p.Gln124=
ENST00000568260.1:c.418C=
ENST00000568777.5:n.3953C=
ENST00000569410.5:c.370C= ENSP00000457125.1:p.Gln124=
ENST00000569509.5:n.375C=
NM_000520.4:c.370C= NP_000511.2:p.Gln124=
NM_000520.5:c.370C= NP_000511.2:p.Gln124=
NM_001318825.1:c.403C= NP_001305754.1:p.Gln135=
NR_134869.1:n.871C=
NM_000520.6:c.370C= MANE Select NP_000511.2:p.Gln124=
NM_001318825.2:c.403C= NP_001305754.1:p.Gln135=
NR_134869.2:n.412C=
NR_134869.3:n.412C=