Canonical Allele Identifier: CA491114020
Gene: HEXA HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.72638221T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72345880T>A , CM000677.2:g.72345880T>A GRCh38
NC_000015.9:g.72638221T>A , CM000677.1:g.72638221T>A GRCh37
NC_000015.8:g.70425275T>A NCBI36
NG_009017.1:g.35300A>T
NG_009017.2:g.35300A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000567027.6:c.*82-330A>T ENSP00000457521.2:n.*82-330A>T
ENST00000682061.1:c.*1438A>T ENSP00000508316.1:n.*1438A>T
ENST00000682064.1:n.1319A>T
ENST00000682177.1:c.1465-330A>T ENSP00000507409.1:n.1465-330A>T
ENST00000682235.1:n.1115A>T
ENST00000682461.1:c.1528-330A>T ENSP00000507308.1:n.1528-330A>T
ENST00000682653.1:n.2096A>T
ENST00000682657.1:c.*929A>T ENSP00000507753.1:n.*929A>T
ENST00000682721.1:c.*1225-330A>T ENSP00000507535.1:n.*1225-330A>T
ENST00000682843.1:c.*1063-330A>T ENSP00000508173.1:n.*1063-330A>T
ENST00000683003.1:c.*929A>T ENSP00000507576.1:n.*929A>T
ENST00000683133.1:c.1606-330A>T ENSP00000508108.1:n.1606-330A>T
ENST00000683243.1:c.*575-330A>T ENSP00000507042.1:n.*575-330A>T
ENST00000683463.1:c.*581A>T ENSP00000507986.1:n.*581A>T
ENST00000683548.1:n.1550A>T
ENST00000683579.1:c.*1320-330A>T ENSP00000506867.1:n.*1320-330A>T
ENST00000683587.1:n.1623A>T
ENST00000683681.1:c.1422-104A>T ENSP00000508110.1:n.1422-104A>T
ENST00000683735.1:c.*1490A>T ENSP00000508336.1:n.*1490A>T
ENST00000683853.1:c.*227-330A>T ENSP00000506834.1:n.*227-330A>T
ENST00000683860.1:c.*212A>T ENSP00000507179.1:n.*212A>T
ENST00000683884.1:c.*419A>T ENSP00000507004.1:n.*419A>T
ENST00000684041.1:c.*351A>T ENSP00000508382.1:n.*351A>T
ENST00000684125.1:c.*82-330A>T ENSP00000507320.1:n.*82-330A>T
ENST00000684203.1:n.3541A>T
ENST00000684231.1:c.*832-330A>T ENSP00000507748.1:n.*832-330A>T
ENST00000684263.1:c.*716A>T ENSP00000508369.1:n.*716A>T
ENST00000684305.1:c.1870-330A>T ENSP00000506819.1:n.1870-330A>T
ENST00000684415.1:c.*643A>T ENSP00000507227.1:n.*643A>T
ENST00000684520.1:c.*351A>T ENSP00000506826.1:n.*351A>T
ENST00000684602.1:c.*1088-330A>T ENSP00000507996.1:n.*1088-330A>T
ENST00000684667.1:c.1753-330A>T ENSP00000507003.1:n.1753-330A>T
ENST00000268097.10:c.1422-330A>T MANE Select ENSP00000268097.6:n.1422-330A>T
ENST00000268097.9:c.1422-330A>T ENSP00000268097.5:n.1422-330A>T
ENST00000379915.4:c.504-330A>T ENSP00000478716.1:n.504-330A>T
ENST00000564677.5:n.10A>T
ENST00000565873.1:n.3A>T
ENST00000566304.5:c.1455-330A>T ENSP00000455114.1:n.1455-330A>T
ENST00000567027.5:c.1037-330A>T
ENST00000567159.5:c.1422-330A>T ENSP00000456489.1:n.1422-330A>T
ENST00000567411.5:c.*943-330A>T ENSP00000455545.1:n.*943-330A>T
ENST00000568777.5:n.6642-330A>T
NM_000520.4:c.1422-330A>T NP_000511.2:n.1422-330A>T
NM_000520.5:c.1422-330A>T NP_000511.2:n.1422-330A>T
NM_001318825.1:c.1455-330A>T NP_001305754.1:n.1455-330A>T
NR_134869.1:n.1666-330A>T
NM_000520.6:c.1422-330A>T MANE Select NP_000511.2:n.1422-330A>T
NM_001318825.2:c.1455-330A>T NP_001305754.1:n.1455-330A>T
NR_134869.2:n.1207-330A>T
NR_134869.3:n.1207-330A>T