Canonical Allele Identifier: CA2186747540
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72355610T= , CM000677.2:g.72355610T= GRCh38
NC_000015.9:g.72647951T= , CM000677.1:g.72647951T= GRCh37
NC_000015.8:g.70435005T= NCBI36
NG_009017.1:g.25570A=
NG_009017.2:g.25570A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000563908.2:n.374A=
ENST00000567027.6:c.361A= ENSP00000457521.2:p.Asn121=
ENST00000568260.2:c.428A= ENSP00000458128.2:n.428A=
ENST00000682061.1:c.*23A= ENSP00000508316.1:n.*23A=
ENST00000682177.1:c.361A= ENSP00000507409.1:p.Asn121=
ENST00000682461.1:c.625A= ENSP00000507308.1:n.625A=
ENST00000682653.1:n.392A=
ENST00000682657.1:c.254-4376A= ENSP00000507753.1:n.254-4376A=
ENST00000682721.1:c.*164A= ENSP00000507535.1:n.*164A=
ENST00000682843.1:c.*259A= ENSP00000508173.1:n.*259A=
ENST00000683003.1:c.361A= ENSP00000507576.1:p.Asn121=
ENST00000683133.1:c.545A= ENSP00000508108.1:n.545A=
ENST00000683228.1:n.392A=
ENST00000683243.1:c.361A= ENSP00000507042.1:p.Asn121=
ENST00000683463.1:c.361A= ENSP00000507986.1:p.Asn121=
ENST00000683548.1:n.392A=
ENST00000683579.1:c.*259A= ENSP00000506867.1:n.*259A=
ENST00000683587.1:n.392A=
ENST00000683681.1:c.361A= ENSP00000508110.1:p.Asn121=
ENST00000683735.1:c.*259A= ENSP00000508336.1:n.*259A=
ENST00000683853.1:c.361A= ENSP00000506834.1:p.Asn121=
ENST00000683860.1:c.361A= ENSP00000507179.1:p.Asn121=
ENST00000683884.1:c.361A= ENSP00000507004.1:p.Asn121=
ENST00000684041.1:c.361A= ENSP00000508382.1:p.Asn121=
ENST00000684125.1:c.361A= ENSP00000507320.1:p.Asn121=
ENST00000684203.1:n.378A=
ENST00000684231.1:c.361A= ENSP00000507748.1:p.Asn121=
ENST00000684263.1:c.361A= ENSP00000508369.1:p.Asn121=
ENST00000684305.1:c.809A= ENSP00000506819.1:n.809A=
ENST00000684415.1:c.361A= ENSP00000507227.1:p.Asn121=
ENST00000684520.1:c.361A= ENSP00000506826.1:p.Asn121=
ENST00000684602.1:c.*185A= ENSP00000507996.1:n.*185A=
ENST00000684667.1:c.692A= ENSP00000507003.1:n.692A=
ENST00000268097.10:c.361A= MANE Select ENSP00000268097.6:p.Asn121=
ENST00000268097.9:c.361A= ENSP00000268097.5:p.Asn121=
ENST00000379915.4:c.361A= ENSP00000478716.1:p.Asn121=
ENST00000563762.5:c.452A= ENSP00000456346.1:n.452A=
ENST00000563908.1:n.358A=
ENST00000566304.5:c.394A= ENSP00000455114.1:p.Asn132=
ENST00000566672.5:c.361A= ENSP00000457037.1:p.Asn121=
ENST00000567027.5:c.233A=
ENST00000567159.5:c.361A= ENSP00000456489.1:p.Asn121=
ENST00000567411.5:c.361A= ENSP00000455545.1:p.Asn121=
ENST00000568260.1:c.409A=
ENST00000568777.5:n.3944A=
ENST00000569410.5:c.361A= ENSP00000457125.1:p.Asn121=
ENST00000569509.5:n.366A=
NM_000520.4:c.361A= NP_000511.2:p.Asn121=
NM_000520.5:c.361A= NP_000511.2:p.Asn121=
NM_001318825.1:c.394A= NP_001305754.1:p.Asn132=
NR_134869.1:n.862A=
NM_000520.6:c.361A= MANE Select NP_000511.2:p.Asn121=
NM_001318825.2:c.394A= NP_001305754.1:p.Asn132=
NR_134869.2:n.403A=
NR_134869.3:n.403A=