Canonical Allele Identifier: CA491117563

Gene: HEXA

Linked Data

• dbSNP Id: rs2140320762
• MyVariant Identifiers: chr15:g.72638992C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72346651C>T , CM000677.2:g.72346651C>T	GRCh38
NC_000015.9:g.72638992C>T , CM000677.1:g.72638992C>T	GRCh37
NC_000015.8:g.70426046C>T	NCBI36
NG_009017.1:g.34529G>A
NG_009017.2:g.34529G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.1074-326G>A	ENSP00000457521.2:n.1074-326G>A
ENST00000682061.1:c.*868G>A	ENSP00000508316.1:n.*868G>A
ENST00000682064.1:n.548G>A
ENST00000682177.1:c.1249G>A	ENSP00000507409.1:n.1249G>A
ENST00000682235.1:n.545G>A
ENST00000682461.1:c.1312G>A	ENSP00000507308.1:n.1312G>A
ENST00000682653.1:n.1526G>A
ENST00000682657.1:c.*484-326G>A	ENSP00000507753.1:n.*484-326G>A
ENST00000682721.1:c.*1009G>A	ENSP00000507535.1:n.*1009G>A
ENST00000682843.1:c.*972-326G>A	ENSP00000508173.1:n.*972-326G>A
ENST00000683003.1:c.*484-326G>A	ENSP00000507576.1:n.*484-326G>A
ENST00000683133.1:c.1390G>A	ENSP00000508108.1:n.1390G>A
ENST00000683243.1:c.*484-326G>A	ENSP00000507042.1:n.*484-326G>A
ENST00000683463.1:c.*11G>A	ENSP00000507986.1:n.*11G>A
ENST00000683548.1:n.1105-326G>A
ENST00000683579.1:c.*1104G>A	ENSP00000506867.1:n.*1104G>A
ENST00000683587.1:n.1178-326G>A
ENST00000683681.1:c.1206G>A	ENSP00000508110.1:p.Lys402=
ENST00000683735.1:c.*1045-326G>A	ENSP00000508336.1:n.*1045-326G>A
ENST00000683853.1:c.*11G>A	ENSP00000506834.1:n.*11G>A
ENST00000683860.1:c.1206G>A	ENSP00000507179.1:p.Lys402=
ENST00000683884.1:c.1147-326G>A	ENSP00000507004.1:n.1147-326G>A
ENST00000684041.1:c.1206G>A	ENSP00000508382.1:p.Lys402=
ENST00000684125.1:c.1074-326G>A	ENSP00000507320.1:n.1074-326G>A
ENST00000684203.1:n.2971G>A
ENST00000684231.1:c.*616G>A	ENSP00000507748.1:n.*616G>A
ENST00000684263.1:c.*146G>A	ENSP00000508369.1:n.*146G>A
ENST00000684305.1:c.1654G>A	ENSP00000506819.1:n.1654G>A
ENST00000684415.1:c.*73G>A	ENSP00000507227.1:n.*73G>A
ENST00000684520.1:c.1206G>A	ENSP00000506826.1:p.Lys402=
ENST00000684602.1:c.*872G>A	ENSP00000507996.1:n.*872G>A
ENST00000684667.1:c.1537G>A	ENSP00000507003.1:n.1537G>A
ENST00000268097.10:c.1206G>A MANE Select	ENSP00000268097.6:p.Lys402=
ENST00000268097.9:c.1206G>A	ENSP00000268097.5:p.Lys402=
ENST00000379915.4:c.413-326G>A	ENSP00000478716.1:n.413-326G>A
ENST00000563762.5:c.826-326G>A	ENSP00000456346.1:n.826-326G>A
ENST00000566304.5:c.1239G>A	ENSP00000455114.1:p.Lys413=
ENST00000566672.5:c.*616G>A	ENSP00000457037.1:n.*616G>A
ENST00000567027.5:c.946-326G>A
ENST00000567159.5:c.1206G>A	ENSP00000456489.1:p.Lys402=
ENST00000567411.5:c.*727G>A	ENSP00000455545.1:n.*727G>A
ENST00000568777.5:n.6551-326G>A
ENST00000569410.5:c.*11G>A	ENSP00000457125.1:n.*11G>A
NM_000520.4:c.1206G>A	NP_000511.2:p.Lys402=
NM_000520.5:c.1206G>A	NP_000511.2:p.Lys402=
NM_001318825.1:c.1239G>A	NP_001305754.1:p.Lys413=
NR_134869.1:n.1575-326G>A
NM_000520.6:c.1206G>A MANE Select	NP_000511.2:p.Lys402=
NM_001318825.2:c.1239G>A	NP_001305754.1:p.Lys413=
NR_134869.2:n.1116-326G>A
NR_134869.3:n.1116-326G>A