Canonical Allele Identifier: CA2186742456
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72343697C= , CM000677.2:g.72343697C= GRCh38
NC_000015.9:g.72636038C= , CM000677.1:g.72636038C= GRCh37
NC_000015.8:g.70423092C= NCBI36
NG_009017.1:g.37483G=
NG_009017.2:g.37483G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682064.1:n.2197G=
ENST00000682235.1:n.1993G=
ENST00000682461.1:c.2076G= ENSP00000507308.1:n.2076G=
ENST00000682653.1:n.4279G=
ENST00000682721.1:c.*1773G= ENSP00000507535.1:n.*1773G=
ENST00000682843.1:c.*1611G= ENSP00000508173.1:n.*1611G=
ENST00000683133.1:c.2154G= ENSP00000508108.1:n.2154G=
ENST00000683243.1:c.*1123G= ENSP00000507042.1:n.*1123G=
ENST00000683463.1:c.*1459G= ENSP00000507986.1:n.*1459G=
ENST00000683548.1:n.2428G=
ENST00000683579.1:c.*1868G= ENSP00000506867.1:n.*1868G=
ENST00000683587.1:n.2501G=
ENST00000683735.1:c.*2368G= ENSP00000508336.1:n.*2368G=
ENST00000683853.1:c.*2080G= ENSP00000506834.1:n.*2080G=
ENST00000684125.1:c.*630G= ENSP00000507320.1:n.*630G=
ENST00000684203.1:n.4419G=
ENST00000684231.1:c.*1380G= ENSP00000507748.1:n.*1380G=
ENST00000684263.1:c.*1594G= ENSP00000508369.1:n.*1594G=
ENST00000684305.1:c.2418G= ENSP00000506819.1:n.2418G=
ENST00000684602.1:c.*1636G= ENSP00000507996.1:n.*1636G=
ENST00000684667.1:c.2301G= ENSP00000507003.1:n.2301G=
ENST00000268097.10:c.*380G= MANE Select ENSP00000268097.6:n.*380G=
ENST00000268097.9:c.*380G= ENSP00000268097.5:n.*380G=
ENST00000379915.4:c.608+1749G= ENSP00000478716.1:n.608+1749G=
NM_000520.4:c.*380G= NP_000511.2:n.*380G=
NM_000520.5:c.*380G= NP_000511.2:n.*380G=
NM_001318825.1:c.*380G= NP_001305754.1:n.*380G=
NM_000520.6:c.*380G= MANE Select NP_000511.2:n.*380G=
NM_001318825.2:c.*380G= NP_001305754.1:n.*380G=