Canonical Allele Identifier: CA491117205

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72638944G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72346603G>C , CM000677.2:g.72346603G>C	GRCh38
NC_000015.9:g.72638944G>C , CM000677.1:g.72638944G>C	GRCh37
NC_000015.8:g.70425998G>C	NCBI36
NG_009017.1:g.34577C>G
NG_009017.2:g.34577C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000567027.6:c.1074-278C>G	ENSP00000457521.2:n.1074-278C>G
ENST00000682061.1:c.*916C>G	ENSP00000508316.1:n.*916C>G
ENST00000682064.1:n.596C>G
ENST00000682177.1:c.1297C>G	ENSP00000507409.1:n.1297C>G
ENST00000682235.1:n.593C>G
ENST00000682461.1:c.1360C>G	ENSP00000507308.1:n.1360C>G
ENST00000682653.1:n.1574C>G
ENST00000682657.1:c.*484-278C>G	ENSP00000507753.1:n.*484-278C>G
ENST00000682721.1:c.*1057C>G	ENSP00000507535.1:n.*1057C>G
ENST00000682843.1:c.*972-278C>G	ENSP00000508173.1:n.*972-278C>G
ENST00000683003.1:c.*484-278C>G	ENSP00000507576.1:n.*484-278C>G
ENST00000683133.1:c.1438C>G	ENSP00000508108.1:n.1438C>G
ENST00000683243.1:c.*484-278C>G	ENSP00000507042.1:n.*484-278C>G
ENST00000683463.1:c.*59C>G	ENSP00000507986.1:n.*59C>G
ENST00000683548.1:n.1105-278C>G
ENST00000683579.1:c.*1152C>G	ENSP00000506867.1:n.*1152C>G
ENST00000683587.1:n.1178-278C>G
ENST00000683681.1:c.1254C>G	ENSP00000508110.1:p.Ala418=
ENST00000683735.1:c.*1045-278C>G	ENSP00000508336.1:n.*1045-278C>G
ENST00000683853.1:c.*59C>G	ENSP00000506834.1:n.*59C>G
ENST00000683860.1:c.1254C>G	ENSP00000507179.1:p.Ala418=
ENST00000683884.1:c.1147-278C>G	ENSP00000507004.1:n.1147-278C>G
ENST00000684041.1:c.1254C>G	ENSP00000508382.1:p.Ala418=
ENST00000684125.1:c.1074-278C>G	ENSP00000507320.1:n.1074-278C>G
ENST00000684203.1:n.3019C>G
ENST00000684231.1:c.*664C>G	ENSP00000507748.1:n.*664C>G
ENST00000684263.1:c.*194C>G	ENSP00000508369.1:n.*194C>G
ENST00000684305.1:c.1702C>G	ENSP00000506819.1:n.1702C>G
ENST00000684415.1:c.*121C>G	ENSP00000507227.1:n.*121C>G
ENST00000684520.1:c.1254C>G	ENSP00000506826.1:p.Ala418=
ENST00000684602.1:c.*920C>G	ENSP00000507996.1:n.*920C>G
ENST00000684667.1:c.1585C>G	ENSP00000507003.1:n.1585C>G
ENST00000268097.10:c.1254C>G MANE Select	ENSP00000268097.6:p.Ala418=
ENST00000268097.9:c.1254C>G	ENSP00000268097.5:p.Ala418=
ENST00000379915.4:c.413-278C>G	ENSP00000478716.1:n.413-278C>G
ENST00000563762.5:c.826-278C>G	ENSP00000456346.1:n.826-278C>G
ENST00000566304.5:c.1287C>G	ENSP00000455114.1:p.Ala429=
ENST00000566672.5:c.*664C>G	ENSP00000457037.1:n.*664C>G
ENST00000567027.5:c.946-278C>G
ENST00000567159.5:c.1254C>G	ENSP00000456489.1:p.Ala418=
ENST00000567411.5:c.*775C>G	ENSP00000455545.1:n.*775C>G
ENST00000568777.5:n.6551-278C>G
ENST00000569410.5:c.*59C>G	ENSP00000457125.1:n.*59C>G
NM_000520.4:c.1254C>G	NP_000511.2:p.Ala418=
NM_000520.5:c.1254C>G	NP_000511.2:p.Ala418=
NM_001318825.1:c.1287C>G	NP_001305754.1:p.Ala429=
NR_134869.1:n.1575-278C>G
NM_000520.6:c.1254C>G MANE Select	NP_000511.2:p.Ala418=
NM_001318825.2:c.1287C>G	NP_001305754.1:p.Ala429=
NR_134869.2:n.1116-278C>G
NR_134869.3:n.1116-278C>G