Canonical Allele Identifier: CA2186743429
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345931T= , CM000677.2:g.72345931T= GRCh38
NC_000015.9:g.72638272T= , CM000677.1:g.72638272T= GRCh37
NC_000015.8:g.70425326T= NCBI36
NG_009017.1:g.35249A=
NG_009017.2:g.35249A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*81+304A= ENSP00000457521.2:n.*81+304A=
ENST00000682061.1:c.*1387A= ENSP00000508316.1:n.*1387A=
ENST00000682064.1:n.1268A=
ENST00000682177.1:c.1464+304A= ENSP00000507409.1:n.1464+304A=
ENST00000682235.1:n.1064A=
ENST00000682461.1:c.1527+304A= ENSP00000507308.1:n.1527+304A=
ENST00000682653.1:n.2045A=
ENST00000682657.1:c.*878A= ENSP00000507753.1:n.*878A=
ENST00000682721.1:c.*1224+304A= ENSP00000507535.1:n.*1224+304A=
ENST00000682843.1:c.*1062+304A= ENSP00000508173.1:n.*1062+304A=
ENST00000683003.1:c.*878A= ENSP00000507576.1:n.*878A=
ENST00000683133.1:c.1605+304A= ENSP00000508108.1:n.1605+304A=
ENST00000683243.1:c.*574+304A= ENSP00000507042.1:n.*574+304A=
ENST00000683463.1:c.*530A= ENSP00000507986.1:n.*530A=
ENST00000683548.1:n.1499A=
ENST00000683579.1:c.*1319+304A= ENSP00000506867.1:n.*1319+304A=
ENST00000683587.1:n.1572A=
ENST00000683681.1:c.1422-155A= ENSP00000508110.1:n.1422-155A=
ENST00000683735.1:c.*1439A= ENSP00000508336.1:n.*1439A=
ENST00000683853.1:c.*226+304A= ENSP00000506834.1:n.*226+304A=
ENST00000683860.1:c.*161A= ENSP00000507179.1:n.*161A=
ENST00000683884.1:c.*368A= ENSP00000507004.1:n.*368A=
ENST00000684041.1:c.*300A= ENSP00000508382.1:n.*300A=
ENST00000684125.1:c.*81+304A= ENSP00000507320.1:n.*81+304A=
ENST00000684203.1:n.3490A=
ENST00000684231.1:c.*831+304A= ENSP00000507748.1:n.*831+304A=
ENST00000684263.1:c.*665A= ENSP00000508369.1:n.*665A=
ENST00000684305.1:c.1869+304A= ENSP00000506819.1:n.1869+304A=
ENST00000684415.1:c.*592A= ENSP00000507227.1:n.*592A=
ENST00000684520.1:c.*300A= ENSP00000506826.1:n.*300A=
ENST00000684602.1:c.*1087+304A= ENSP00000507996.1:n.*1087+304A=
ENST00000684667.1:c.1752+304A= ENSP00000507003.1:n.1752+304A=
ENST00000268097.10:c.1421+304A= MANE Select ENSP00000268097.6:n.1421+304A=
ENST00000268097.9:c.1421+304A= ENSP00000268097.5:n.1421+304A=
ENST00000379915.4:c.503+304A= ENSP00000478716.1:n.503+304A=
ENST00000566304.5:c.1454+304A= ENSP00000455114.1:n.1454+304A=
ENST00000567027.5:c.1036+304A=
ENST00000567159.5:c.1421+304A= ENSP00000456489.1:n.1421+304A=
ENST00000567411.5:c.*942+304A= ENSP00000455545.1:n.*942+304A=
ENST00000568777.5:n.6641+304A=
NM_000520.4:c.1421+304A= NP_000511.2:n.1421+304A=
NM_000520.5:c.1421+304A= NP_000511.2:n.1421+304A=
NM_001318825.1:c.1454+304A= NP_001305754.1:n.1454+304A=
NR_134869.1:n.1665+304A=
NM_000520.6:c.1421+304A= MANE Select NP_000511.2:n.1421+304A=
NM_001318825.2:c.1454+304A= NP_001305754.1:n.1454+304A=
NR_134869.2:n.1206+304A=
NR_134869.3:n.1206+304A=