Canonical Allele Identifier: CA393062027
Gene: HEXA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72348136T>G , CM000677.2:g.72348136T>G GRCh38
NC_000015.9:g.72640477T>G , CM000677.1:g.72640477T>G GRCh37
NC_000015.8:g.70427531T>G NCBI36
NG_009017.1:g.33044A>C
NG_009017.2:g.33044A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000563908.2:n.3333-2A>C
ENST00000567027.6:c.987-2A>C ENSP00000457521.2:n.987-2A>C
ENST00000682061.1:c.*649-2A>C ENSP00000508316.1:n.*649-2A>C
ENST00000682177.1:c.1030-2A>C ENSP00000507409.1:n.1030-2A>C
ENST00000682461.1:c.1093-2A>C ENSP00000507308.1:n.1093-2A>C
ENST00000682653.1:n.1018-2A>C
ENST00000682657.1:c.*397-2A>C ENSP00000507753.1:n.*397-2A>C
ENST00000682721.1:c.*790-2A>C ENSP00000507535.1:n.*790-2A>C
ENST00000682843.1:c.*885-2A>C ENSP00000508173.1:n.*885-2A>C
ENST00000683003.1:c.*397-2A>C ENSP00000507576.1:n.*397-2A>C
ENST00000683133.1:c.1171-2A>C ENSP00000508108.1:n.1171-2A>C
ENST00000683228.1:n.1018-2A>C
ENST00000683243.1:c.*397-2A>C ENSP00000507042.1:n.*397-2A>C
ENST00000683463.1:c.987-2A>C ENSP00000507986.1:n.987-2A>C
ENST00000683548.1:n.1018-2A>C
ENST00000683579.1:c.*885-2A>C ENSP00000506867.1:n.*885-2A>C
ENST00000683587.1:n.1018-2A>C
ENST00000683681.1:c.987-2A>C ENSP00000508110.1:n.987-2A>C
ENST00000683735.1:c.*885-2A>C ENSP00000508336.1:n.*885-2A>C
ENST00000683742.1:n.818-2A>C
ENST00000683853.1:c.987-2A>C ENSP00000506834.1:n.987-2A>C
ENST00000683860.1:c.987-2A>C ENSP00000507179.1:n.987-2A>C
ENST00000683884.1:c.987-2A>C ENSP00000507004.1:n.987-2A>C
ENST00000684041.1:c.987-2A>C ENSP00000508382.1:n.987-2A>C
ENST00000684125.1:c.987-2A>C ENSP00000507320.1:n.987-2A>C
ENST00000684203.1:n.2825-2A>C
ENST00000684231.1:c.*397-2A>C ENSP00000507748.1:n.*397-2A>C
ENST00000684263.1:c.987-2A>C ENSP00000508369.1:n.987-2A>C
ENST00000684305.1:c.1435-2A>C ENSP00000506819.1:n.1435-2A>C
ENST00000684415.1:c.987-2A>C ENSP00000507227.1:n.987-2A>C
ENST00000684520.1:c.987-2A>C ENSP00000506826.1:n.987-2A>C
ENST00000684602.1:c.*653-2A>C ENSP00000507996.1:n.*653-2A>C
ENST00000684667.1:c.1318-2A>C ENSP00000507003.1:n.1318-2A>C
ENST00000268097.10:c.987-2A>C MANE Select ENSP00000268097.6:n.987-2A>C
ENST00000268097.9:c.987-2A>C ENSP00000268097.5:n.987-2A>C
ENST00000379915.4:c.413-1811A>C ENSP00000478716.1:n.413-1811A>C
ENST00000563762.5:c.739-2A>C ENSP00000456346.1:n.739-2A>C
ENST00000566304.5:c.1020-2A>C ENSP00000455114.1:n.1020-2A>C
ENST00000566672.5:c.*397-2A>C ENSP00000457037.1:n.*397-2A>C
ENST00000567027.5:c.859-2A>C
ENST00000567159.5:c.987-2A>C ENSP00000456489.1:n.987-2A>C
ENST00000567411.5:c.*508-2A>C ENSP00000455545.1:n.*508-2A>C
ENST00000568777.5:n.6391-2A>C
ENST00000569410.5:c.987-2A>C ENSP00000457125.1:n.987-2A>C
NM_000520.4:c.987-2A>C NP_000511.2:n.987-2A>C
NM_000520.5:c.987-2A>C NP_000511.2:n.987-2A>C
NM_001318825.1:c.1020-2A>C NP_001305754.1:n.1020-2A>C
NR_134869.1:n.1488-2A>C
NM_000520.6:c.987-2A>C MANE Select NP_000511.2:n.987-2A>C
NM_001318825.2:c.1020-2A>C NP_001305754.1:n.1020-2A>C
NR_134869.2:n.1029-2A>C
NR_134869.3:n.1029-2A>C