Canonical Allele Identifier: CA491113616

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72638184A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345843A>T , CM000677.2:g.72345843A>T	GRCh38
NC_000015.9:g.72638184A>T , CM000677.1:g.72638184A>T	GRCh37
NC_000015.8:g.70425238A>T	NCBI36
NG_009017.1:g.35337T>A
NG_009017.2:g.35337T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567027.6:c.*82-293T>A	ENSP00000457521.2:n.*82-293T>A
ENST00000682061.1:c.*1475T>A	ENSP00000508316.1:n.*1475T>A
ENST00000682064.1:n.1356T>A
ENST00000682177.1:c.1465-293T>A	ENSP00000507409.1:n.1465-293T>A
ENST00000682235.1:n.1152T>A
ENST00000682461.1:c.1528-293T>A	ENSP00000507308.1:n.1528-293T>A
ENST00000682653.1:n.2133T>A
ENST00000682657.1:c.*966T>A	ENSP00000507753.1:n.*966T>A
ENST00000682721.1:c.*1225-293T>A	ENSP00000507535.1:n.*1225-293T>A
ENST00000682843.1:c.*1063-293T>A	ENSP00000508173.1:n.*1063-293T>A
ENST00000683003.1:c.*966T>A	ENSP00000507576.1:n.*966T>A
ENST00000683133.1:c.1606-293T>A	ENSP00000508108.1:n.1606-293T>A
ENST00000683243.1:c.*575-293T>A	ENSP00000507042.1:n.*575-293T>A
ENST00000683463.1:c.*618T>A	ENSP00000507986.1:n.*618T>A
ENST00000683548.1:n.1587T>A
ENST00000683579.1:c.*1320-293T>A	ENSP00000506867.1:n.*1320-293T>A
ENST00000683587.1:n.1660T>A
ENST00000683681.1:c.1422-67T>A	ENSP00000508110.1:n.1422-67T>A
ENST00000683735.1:c.*1527T>A	ENSP00000508336.1:n.*1527T>A
ENST00000683853.1:c.*227-293T>A	ENSP00000506834.1:n.*227-293T>A
ENST00000683860.1:c.*249T>A	ENSP00000507179.1:n.*249T>A
ENST00000683884.1:c.*456T>A	ENSP00000507004.1:n.*456T>A
ENST00000684041.1:c.*388T>A	ENSP00000508382.1:n.*388T>A
ENST00000684125.1:c.*82-293T>A	ENSP00000507320.1:n.*82-293T>A
ENST00000684203.1:n.3578T>A
ENST00000684231.1:c.*832-293T>A	ENSP00000507748.1:n.*832-293T>A
ENST00000684263.1:c.*753T>A	ENSP00000508369.1:n.*753T>A
ENST00000684305.1:c.1870-293T>A	ENSP00000506819.1:n.1870-293T>A
ENST00000684415.1:c.*680T>A	ENSP00000507227.1:n.*680T>A
ENST00000684520.1:c.*388T>A	ENSP00000506826.1:n.*388T>A
ENST00000684602.1:c.*1088-293T>A	ENSP00000507996.1:n.*1088-293T>A
ENST00000684667.1:c.1753-293T>A	ENSP00000507003.1:n.1753-293T>A
ENST00000268097.10:c.1422-293T>A MANE Select	ENSP00000268097.6:n.1422-293T>A
ENST00000268097.9:c.1422-293T>A	ENSP00000268097.5:n.1422-293T>A
ENST00000379915.4:c.504-293T>A	ENSP00000478716.1:n.504-293T>A
ENST00000564677.5:n.47T>A
ENST00000565873.1:n.40T>A
ENST00000566304.5:c.1455-293T>A	ENSP00000455114.1:n.1455-293T>A
ENST00000567027.5:c.1037-293T>A
ENST00000567159.5:c.1422-293T>A	ENSP00000456489.1:n.1422-293T>A
ENST00000567411.5:c.*943-293T>A	ENSP00000455545.1:n.*943-293T>A
ENST00000568777.5:n.6642-293T>A
NM_000520.4:c.1422-293T>A	NP_000511.2:n.1422-293T>A
NM_000520.5:c.1422-293T>A	NP_000511.2:n.1422-293T>A
NM_001318825.1:c.1455-293T>A	NP_001305754.1:n.1455-293T>A
NR_134869.1:n.1666-293T>A
NM_000520.6:c.1422-293T>A MANE Select	NP_000511.2:n.1422-293T>A
NM_001318825.2:c.1455-293T>A	NP_001305754.1:n.1455-293T>A
NR_134869.2:n.1207-293T>A
NR_134869.3:n.1207-293T>A