Canonical Allele Identifier: CA491113684
Gene: HEXA HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.72638196A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345855A>C , CM000677.2:g.72345855A>C GRCh38
NC_000015.9:g.72638196A>C , CM000677.1:g.72638196A>C GRCh37
NC_000015.8:g.70425250A>C NCBI36
NG_009017.1:g.35325T>G
NG_009017.2:g.35325T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*82-305T>G ENSP00000457521.2:n.*82-305T>G
ENST00000682061.1:c.*1463T>G ENSP00000508316.1:n.*1463T>G
ENST00000682064.1:n.1344T>G
ENST00000682177.1:c.1465-305T>G ENSP00000507409.1:n.1465-305T>G
ENST00000682235.1:n.1140T>G
ENST00000682461.1:c.1528-305T>G ENSP00000507308.1:n.1528-305T>G
ENST00000682653.1:n.2121T>G
ENST00000682657.1:c.*954T>G ENSP00000507753.1:n.*954T>G
ENST00000682721.1:c.*1225-305T>G ENSP00000507535.1:n.*1225-305T>G
ENST00000682843.1:c.*1063-305T>G ENSP00000508173.1:n.*1063-305T>G
ENST00000683003.1:c.*954T>G ENSP00000507576.1:n.*954T>G
ENST00000683133.1:c.1606-305T>G ENSP00000508108.1:n.1606-305T>G
ENST00000683243.1:c.*575-305T>G ENSP00000507042.1:n.*575-305T>G
ENST00000683463.1:c.*606T>G ENSP00000507986.1:n.*606T>G
ENST00000683548.1:n.1575T>G
ENST00000683579.1:c.*1320-305T>G ENSP00000506867.1:n.*1320-305T>G
ENST00000683587.1:n.1648T>G
ENST00000683681.1:c.1422-79T>G ENSP00000508110.1:n.1422-79T>G
ENST00000683735.1:c.*1515T>G ENSP00000508336.1:n.*1515T>G
ENST00000683853.1:c.*227-305T>G ENSP00000506834.1:n.*227-305T>G
ENST00000683860.1:c.*237T>G ENSP00000507179.1:n.*237T>G
ENST00000683884.1:c.*444T>G ENSP00000507004.1:n.*444T>G
ENST00000684041.1:c.*376T>G ENSP00000508382.1:n.*376T>G
ENST00000684125.1:c.*82-305T>G ENSP00000507320.1:n.*82-305T>G
ENST00000684203.1:n.3566T>G
ENST00000684231.1:c.*832-305T>G ENSP00000507748.1:n.*832-305T>G
ENST00000684263.1:c.*741T>G ENSP00000508369.1:n.*741T>G
ENST00000684305.1:c.1870-305T>G ENSP00000506819.1:n.1870-305T>G
ENST00000684415.1:c.*668T>G ENSP00000507227.1:n.*668T>G
ENST00000684520.1:c.*376T>G ENSP00000506826.1:n.*376T>G
ENST00000684602.1:c.*1088-305T>G ENSP00000507996.1:n.*1088-305T>G
ENST00000684667.1:c.1753-305T>G ENSP00000507003.1:n.1753-305T>G
ENST00000268097.10:c.1422-305T>G MANE Select ENSP00000268097.6:n.1422-305T>G
ENST00000268097.9:c.1422-305T>G ENSP00000268097.5:n.1422-305T>G
ENST00000379915.4:c.504-305T>G ENSP00000478716.1:n.504-305T>G
ENST00000564677.5:n.35T>G
ENST00000565873.1:n.28T>G
ENST00000566304.5:c.1455-305T>G ENSP00000455114.1:n.1455-305T>G
ENST00000567027.5:c.1037-305T>G
ENST00000567159.5:c.1422-305T>G ENSP00000456489.1:n.1422-305T>G
ENST00000567411.5:c.*943-305T>G ENSP00000455545.1:n.*943-305T>G
ENST00000568777.5:n.6642-305T>G
NM_000520.4:c.1422-305T>G NP_000511.2:n.1422-305T>G
NM_000520.5:c.1422-305T>G NP_000511.2:n.1422-305T>G
NM_001318825.1:c.1455-305T>G NP_001305754.1:n.1455-305T>G
NR_134869.1:n.1666-305T>G
NM_000520.6:c.1422-305T>G MANE Select NP_000511.2:n.1422-305T>G
NM_001318825.2:c.1455-305T>G NP_001305754.1:n.1455-305T>G
NR_134869.2:n.1207-305T>G
NR_134869.3:n.1207-305T>G