Canonical Allele Identifier: CA491110997

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72637774A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345433A>C , CM000677.2:g.72345433A>C	GRCh38
NC_000015.9:g.72637774A>C , CM000677.1:g.72637774A>C	GRCh37
NC_000015.8:g.70424828A>C	NCBI36
NG_009017.1:g.35747T>G
NG_009017.2:g.35747T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*199T>G	ENSP00000457521.2:n.*199T>G
ENST00000682061.1:c.*1885T>G	ENSP00000508316.1:n.*1885T>G
ENST00000682064.1:n.1753+13T>G
ENST00000682177.1:c.1582T>G	ENSP00000507409.1:n.1582T>G
ENST00000682235.1:n.1549+13T>G
ENST00000682461.1:c.1632+13T>G	ENSP00000507308.1:n.1632+13T>G
ENST00000682653.1:n.2543T>G
ENST00000682657.1:c.*1376T>G	ENSP00000507753.1:n.*1376T>G
ENST00000682721.1:c.*1329+13T>G	ENSP00000507535.1:n.*1329+13T>G
ENST00000682843.1:c.*1167+13T>G	ENSP00000508173.1:n.*1167+13T>G
ENST00000683003.1:c.*1376T>G	ENSP00000507576.1:n.*1376T>G
ENST00000683133.1:c.1710+13T>G	ENSP00000508108.1:n.1710+13T>G
ENST00000683243.1:c.*679+13T>G	ENSP00000507042.1:n.*679+13T>G
ENST00000683463.1:c.*1015+13T>G	ENSP00000507986.1:n.*1015+13T>G
ENST00000683548.1:n.1984+13T>G
ENST00000683579.1:c.*1424+13T>G	ENSP00000506867.1:n.*1424+13T>G
ENST00000683587.1:n.2057+13T>G
ENST00000683681.1:c.*204+13T>G	ENSP00000508110.1:n.*204+13T>G
ENST00000683735.1:c.*1924+13T>G	ENSP00000508336.1:n.*1924+13T>G
ENST00000683853.1:c.*344T>G	ENSP00000506834.1:n.*344T>G
ENST00000683860.1:c.*646+13T>G	ENSP00000507179.1:n.*646+13T>G
ENST00000683884.1:c.*866T>G	ENSP00000507004.1:n.*866T>G
ENST00000684125.1:c.*186+13T>G	ENSP00000507320.1:n.*186+13T>G
ENST00000684203.1:n.3975+13T>G
ENST00000684231.1:c.*936+13T>G	ENSP00000507748.1:n.*936+13T>G
ENST00000684263.1:c.*1150+13T>G	ENSP00000508369.1:n.*1150+13T>G
ENST00000684305.1:c.1974+13T>G	ENSP00000506819.1:n.1974+13T>G
ENST00000684415.1:c.*1090T>G	ENSP00000507227.1:n.*1090T>G
ENST00000684520.1:c.*798T>G	ENSP00000506826.1:n.*798T>G
ENST00000684602.1:c.*1192+13T>G	ENSP00000507996.1:n.*1192+13T>G
ENST00000684667.1:c.1857+13T>G	ENSP00000507003.1:n.1857+13T>G
ENST00000268097.10:c.1526+13T>G MANE Select	ENSP00000268097.6:n.1526+13T>G
ENST00000268097.9:c.1526+13T>G	ENSP00000268097.5:n.1526+13T>G
ENST00000379915.4:c.608+13T>G	ENSP00000478716.1:n.608+13T>G
ENST00000564677.5:n.318+13T>G
ENST00000565873.1:n.437+13T>G
ENST00000566304.5:c.1559+13T>G	ENSP00000455114.1:n.1559+13T>G
ENST00000567027.5:c.1154T>G
ENST00000567159.5:c.*9T>G	ENSP00000456489.1:n.*9T>G
ENST00000567411.5:c.*1047+13T>G	ENSP00000455545.1:n.*1047+13T>G
ENST00000568777.5:n.6759T>G
ENST00000569116.1:n.246T>G
NM_000520.4:c.1526+13T>G	NP_000511.2:n.1526+13T>G
NM_000520.5:c.1526+13T>G	NP_000511.2:n.1526+13T>G
NM_001318825.1:c.1559+13T>G	NP_001305754.1:n.1559+13T>G
NR_134869.1:n.1783T>G
NM_000520.6:c.1526+13T>G MANE Select	NP_000511.2:n.1526+13T>G
NM_001318825.2:c.1559+13T>G	NP_001305754.1:n.1559+13T>G
NR_134869.2:n.1324T>G
NR_134869.3:n.1324T>G