Canonical Allele Identifier: CA393059302

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72638639A>C (hg19) ; chr15:g.72346298A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72346298A>C , CM000677.2:g.72346298A>C	GRCh38
NC_000015.9:g.72638639A>C , CM000677.1:g.72638639A>C	GRCh37
NC_000015.8:g.70425693A>C	NCBI36
NG_009017.1:g.34882T>G
NG_009017.2:g.34882T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*18T>G	ENSP00000457521.2:n.*18T>G
ENST00000682061.1:c.*1020T>G	ENSP00000508316.1:n.*1020T>G
ENST00000682064.1:n.901T>G
ENST00000682177.1:c.1401T>G	ENSP00000507409.1:n.1401T>G
ENST00000682235.1:n.697T>G
ENST00000682461.1:c.1464T>G	ENSP00000507308.1:n.1464T>G
ENST00000682653.1:n.1678T>G
ENST00000682657.1:c.*511T>G	ENSP00000507753.1:n.*511T>G
ENST00000682721.1:c.*1161T>G	ENSP00000507535.1:n.*1161T>G
ENST00000682843.1:c.*999T>G	ENSP00000508173.1:n.*999T>G
ENST00000683003.1:c.*511T>G	ENSP00000507576.1:n.*511T>G
ENST00000683133.1:c.1542T>G	ENSP00000508108.1:n.1542T>G
ENST00000683243.1:c.*511T>G	ENSP00000507042.1:n.*511T>G
ENST00000683463.1:c.*163T>G	ENSP00000507986.1:n.*163T>G
ENST00000683548.1:n.1132T>G
ENST00000683579.1:c.*1256T>G	ENSP00000506867.1:n.*1256T>G
ENST00000683587.1:n.1205T>G
ENST00000683681.1:c.1358T>G	ENSP00000508110.1:p.Ile453Ser
ENST00000683735.1:c.*1072T>G	ENSP00000508336.1:n.*1072T>G
ENST00000683853.1:c.*163T>G	ENSP00000506834.1:n.*163T>G
ENST00000683860.1:c.1358T>G	ENSP00000507179.1:p.Ile453Ser
ENST00000683884.1:c.*1T>G	ENSP00000507004.1:n.*1T>G
ENST00000684041.1:c.1358T>G	ENSP00000508382.1:p.Ile453Ser
ENST00000684125.1:c.*18T>G	ENSP00000507320.1:n.*18T>G
ENST00000684203.1:n.3123T>G
ENST00000684231.1:c.*768T>G	ENSP00000507748.1:n.*768T>G
ENST00000684263.1:c.*298T>G	ENSP00000508369.1:n.*298T>G
ENST00000684305.1:c.1806T>G	ENSP00000506819.1:n.1806T>G
ENST00000684415.1:c.*225T>G	ENSP00000507227.1:n.*225T>G
ENST00000684520.1:c.1358T>G	ENSP00000506826.1:p.Ile453Ser
ENST00000684602.1:c.*1024T>G	ENSP00000507996.1:n.*1024T>G
ENST00000684667.1:c.1689T>G	ENSP00000507003.1:n.1689T>G
ENST00000268097.10:c.1358T>G MANE Select	ENSP00000268097.6:p.Ile453Ser
ENST00000268097.9:c.1358T>G	ENSP00000268097.5:p.Ile453Ser
ENST00000379915.4:c.440T>G	ENSP00000478716.1:p.Ile147Ser
ENST00000563762.5:c.853T>G	ENSP00000456346.1:n.853T>G
ENST00000566304.5:c.1391T>G	ENSP00000455114.1:p.Ile464Ser
ENST00000566672.5:c.*768T>G	ENSP00000457037.1:n.*768T>G
ENST00000567027.5:c.973T>G
ENST00000567159.5:c.1358T>G	ENSP00000456489.1:p.Ile453Ser
ENST00000567411.5:c.*879T>G	ENSP00000455545.1:n.*879T>G
ENST00000568777.5:n.6578T>G
ENST00000569410.5:c.*163T>G	ENSP00000457125.1:n.*163T>G
NM_000520.4:c.1358T>G	NP_000511.2:p.Ile453Ser
NM_000520.5:c.1358T>G	NP_000511.2:p.Ile453Ser
NM_001318825.1:c.1391T>G	NP_001305754.1:p.Ile464Ser
NR_134869.1:n.1602T>G
NM_000520.6:c.1358T>G MANE Select	NP_000511.2:p.Ile453Ser
NM_001318825.2:c.1391T>G	NP_001305754.1:p.Ile464Ser
NR_134869.2:n.1143T>G
NR_134869.3:n.1143T>G