Canonical Allele Identifier: CA2186743279
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345508C= , CM000677.2:g.72345508C= GRCh38
NC_000015.9:g.72637849C= , CM000677.1:g.72637849C= GRCh37
NC_000015.8:g.70424903C= NCBI36
NG_009017.1:g.35672G=
NG_009017.2:g.35672G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*124G= ENSP00000457521.2:n.*124G=
ENST00000682061.1:c.*1810G= ENSP00000508316.1:n.*1810G=
ENST00000682064.1:n.1691G=
ENST00000682177.1:c.1507G= ENSP00000507409.1:n.1507G=
ENST00000682235.1:n.1487G=
ENST00000682461.1:c.1570G= ENSP00000507308.1:n.1570G=
ENST00000682653.1:n.2468G=
ENST00000682657.1:c.*1301G= ENSP00000507753.1:n.*1301G=
ENST00000682721.1:c.*1267G= ENSP00000507535.1:n.*1267G=
ENST00000682843.1:c.*1105G= ENSP00000508173.1:n.*1105G=
ENST00000683003.1:c.*1301G= ENSP00000507576.1:n.*1301G=
ENST00000683133.1:c.1648G= ENSP00000508108.1:n.1648G=
ENST00000683243.1:c.*617G= ENSP00000507042.1:n.*617G=
ENST00000683463.1:c.*953G= ENSP00000507986.1:n.*953G=
ENST00000683548.1:n.1922G=
ENST00000683579.1:c.*1362G= ENSP00000506867.1:n.*1362G=
ENST00000683587.1:n.1995G=
ENST00000683681.1:c.*142G= ENSP00000508110.1:n.*142G=
ENST00000683735.1:c.*1862G= ENSP00000508336.1:n.*1862G=
ENST00000683853.1:c.*269G= ENSP00000506834.1:n.*269G=
ENST00000683860.1:c.*584G= ENSP00000507179.1:n.*584G=
ENST00000683884.1:c.*791G= ENSP00000507004.1:n.*791G=
ENST00000684041.1:c.*597G= ENSP00000508382.1:n.*597G=
ENST00000684125.1:c.*124G= ENSP00000507320.1:n.*124G=
ENST00000684203.1:n.3913G=
ENST00000684231.1:c.*874G= ENSP00000507748.1:n.*874G=
ENST00000684263.1:c.*1088G= ENSP00000508369.1:n.*1088G=
ENST00000684305.1:c.1912G= ENSP00000506819.1:n.1912G=
ENST00000684415.1:c.*1015G= ENSP00000507227.1:n.*1015G=
ENST00000684520.1:c.*723G= ENSP00000506826.1:n.*723G=
ENST00000684602.1:c.*1130G= ENSP00000507996.1:n.*1130G=
ENST00000684667.1:c.1795G= ENSP00000507003.1:n.1795G=
ENST00000268097.10:c.1464G= MANE Select ENSP00000268097.6:p.Lys488=
ENST00000268097.9:c.1464G= ENSP00000268097.5:p.Lys488=
ENST00000379915.4:c.546G= ENSP00000478716.1:p.Lys182=
ENST00000564677.5:n.256G=
ENST00000565873.1:n.375G=
ENST00000566304.5:c.1497G= ENSP00000455114.1:p.Lys499=
ENST00000567027.5:c.1079G=
ENST00000567159.5:c.1464G= ENSP00000456489.1:p.Lys488=
ENST00000567411.5:c.*985G= ENSP00000455545.1:n.*985G=
ENST00000568777.5:n.6684G=
ENST00000569116.1:n.171G=
NM_000520.4:c.1464G= NP_000511.2:p.Lys488=
NM_000520.5:c.1464G= NP_000511.2:p.Lys488=
NM_001318825.1:c.1497G= NP_001305754.1:p.Lys499=
NR_134869.1:n.1708G=
NM_000520.6:c.1464G= MANE Select NP_000511.2:p.Lys488=
NM_001318825.2:c.1497G= NP_001305754.1:p.Lys499=
NR_134869.2:n.1249G=
NR_134869.3:n.1249G=