Canonical Allele Identifier: CA393063008
Gene: HEXA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72350529G>C , CM000677.2:g.72350529G>C GRCh38
NC_000015.9:g.72642870G>C , CM000677.1:g.72642870G>C GRCh37
NC_000015.8:g.70429924G>C NCBI36
NG_009017.1:g.30651C>G
NG_009017.2:g.30651C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000563908.2:n.3140C>G
ENST00000567027.6:c.794C>G ENSP00000457521.2:p.Ser265Cys
ENST00000682061.1:c.*456C>G ENSP00000508316.1:n.*456C>G
ENST00000682177.1:c.837C>G ENSP00000507409.1:n.837C>G
ENST00000682461.1:c.900C>G ENSP00000507308.1:n.900C>G
ENST00000682653.1:n.825C>G
ENST00000682657.1:c.*204C>G ENSP00000507753.1:n.*204C>G
ENST00000682721.1:c.*597C>G ENSP00000507535.1:n.*597C>G
ENST00000682843.1:c.*692C>G ENSP00000508173.1:n.*692C>G
ENST00000683003.1:c.*204C>G ENSP00000507576.1:n.*204C>G
ENST00000683133.1:c.978C>G ENSP00000508108.1:n.978C>G
ENST00000683228.1:n.825C>G
ENST00000683243.1:c.*204C>G ENSP00000507042.1:n.*204C>G
ENST00000683463.1:c.794C>G ENSP00000507986.1:p.Ser265Cys
ENST00000683548.1:n.825C>G
ENST00000683579.1:c.*692C>G ENSP00000506867.1:n.*692C>G
ENST00000683587.1:n.825C>G
ENST00000683681.1:c.794C>G ENSP00000508110.1:p.Ser265Cys
ENST00000683735.1:c.*692C>G ENSP00000508336.1:n.*692C>G
ENST00000683742.1:n.625C>G
ENST00000683853.1:c.794C>G ENSP00000506834.1:p.Ser265Cys
ENST00000683860.1:c.794C>G ENSP00000507179.1:p.Ser265Cys
ENST00000683884.1:c.794C>G ENSP00000507004.1:p.Ser265Cys
ENST00000684041.1:c.794C>G ENSP00000508382.1:p.Ser265Cys
ENST00000684125.1:c.794C>G ENSP00000507320.1:p.Ser265Cys
ENST00000684203.1:n.2632C>G
ENST00000684231.1:c.*204C>G ENSP00000507748.1:n.*204C>G
ENST00000684263.1:c.794C>G ENSP00000508369.1:p.Ser265Cys
ENST00000684305.1:c.1242C>G ENSP00000506819.1:n.1242C>G
ENST00000684415.1:c.794C>G ENSP00000507227.1:p.Ser265Cys
ENST00000684520.1:c.794C>G ENSP00000506826.1:p.Ser265Cys
ENST00000684602.1:c.*460C>G ENSP00000507996.1:n.*460C>G
ENST00000684667.1:c.1125C>G ENSP00000507003.1:n.1125C>G
ENST00000268097.10:c.794C>G MANE Select ENSP00000268097.6:p.Ser265Cys
ENST00000268097.9:c.794C>G ENSP00000268097.5:p.Ser265Cys
ENST00000379915.4:c.413-4204C>G ENSP00000478716.1:n.413-4204C>G
ENST00000563762.5:c.727C>G ENSP00000456346.1:n.727C>G
ENST00000566304.5:c.827C>G ENSP00000455114.1:p.Ser276Cys
ENST00000566672.5:c.*204C>G ENSP00000457037.1:n.*204C>G
ENST00000567027.5:c.666C>G
ENST00000567159.5:c.794C>G ENSP00000456489.1:p.Ser265Cys
ENST00000567411.5:c.*315C>G ENSP00000455545.1:n.*315C>G
ENST00000568777.5:n.6198C>G
ENST00000569410.5:c.794C>G ENSP00000457125.1:p.Ser265Cys
NM_000520.4:c.794C>G NP_000511.2:p.Ser265Cys
NM_000520.5:c.794C>G NP_000511.2:p.Ser265Cys
NM_001318825.1:c.827C>G NP_001305754.1:p.Ser276Cys
NR_134869.1:n.1295C>G
NM_000520.6:c.794C>G MANE Select NP_000511.2:p.Ser265Cys
NM_001318825.2:c.827C>G NP_001305754.1:p.Ser276Cys
NR_134869.2:n.836C>G
NR_134869.3:n.836C>G