Canonical Allele Identifier: CA393061618

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72640035T>A (hg19) ; chr15:g.72347694T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72347694T>A , CM000677.2:g.72347694T>A	GRCh38
NC_000015.9:g.72640035T>A , CM000677.1:g.72640035T>A	GRCh37
NC_000015.8:g.70427089T>A	NCBI36
NG_009017.1:g.33486A>T
NG_009017.2:g.33486A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000567027.6:c.1073+354A>T	ENSP00000457521.2:n.1073+354A>T
ENST00000682061.1:c.*800A>T	ENSP00000508316.1:n.*800A>T
ENST00000682177.1:c.1181A>T	ENSP00000507409.1:n.1181A>T
ENST00000682461.1:c.1244A>T	ENSP00000507308.1:n.1244A>T
ENST00000682653.1:n.1458A>T
ENST00000682657.1:c.*483+354A>T	ENSP00000507753.1:n.*483+354A>T
ENST00000682721.1:c.*941A>T	ENSP00000507535.1:n.*941A>T
ENST00000682843.1:c.*971+354A>T	ENSP00000508173.1:n.*971+354A>T
ENST00000683003.1:c.*483+354A>T	ENSP00000507576.1:n.*483+354A>T
ENST00000683133.1:c.1322A>T	ENSP00000508108.1:n.1322A>T
ENST00000683228.1:n.1169A>T
ENST00000683243.1:c.*483+354A>T	ENSP00000507042.1:n.*483+354A>T
ENST00000683463.1:c.1073+354A>T	ENSP00000507986.1:n.1073+354A>T
ENST00000683548.1:n.1104+354A>T
ENST00000683579.1:c.*1036A>T	ENSP00000506867.1:n.*1036A>T
ENST00000683587.1:n.1169A>T
ENST00000683681.1:c.1138A>T	ENSP00000508110.1:p.Lys380Ter
ENST00000683735.1:c.*1036A>T	ENSP00000508336.1:n.*1036A>T
ENST00000683742.1:n.969A>T
ENST00000683853.1:c.1073+354A>T	ENSP00000506834.1:n.1073+354A>T
ENST00000683860.1:c.1138A>T	ENSP00000507179.1:p.Lys380Ter
ENST00000683884.1:c.1138A>T	ENSP00000507004.1:p.Lys380Ter
ENST00000684041.1:c.1138A>T	ENSP00000508382.1:p.Lys380Ter
ENST00000684125.1:c.1073+354A>T	ENSP00000507320.1:n.1073+354A>T
ENST00000684203.1:n.2911+354A>T
ENST00000684231.1:c.*548A>T	ENSP00000507748.1:n.*548A>T
ENST00000684263.1:c.*78A>T	ENSP00000508369.1:n.*78A>T
ENST00000684305.1:c.1586A>T	ENSP00000506819.1:n.1586A>T
ENST00000684415.1:c.*13+337A>T	ENSP00000507227.1:n.*13+337A>T
ENST00000684520.1:c.1138A>T	ENSP00000506826.1:p.Lys380Ter
ENST00000684602.1:c.*804A>T	ENSP00000507996.1:n.*804A>T
ENST00000684667.1:c.1469A>T	ENSP00000507003.1:n.1469A>T
ENST00000268097.10:c.1138A>T MANE Select	ENSP00000268097.6:p.Lys380Ter
ENST00000268097.9:c.1138A>T	ENSP00000268097.5:p.Lys380Ter
ENST00000379915.4:c.413-1369A>T	ENSP00000478716.1:n.413-1369A>T
ENST00000563762.5:c.825+354A>T	ENSP00000456346.1:n.825+354A>T
ENST00000566304.5:c.1171A>T	ENSP00000455114.1:p.Lys391Ter
ENST00000566672.5:c.*548A>T	ENSP00000457037.1:n.*548A>T
ENST00000567027.5:c.945+354A>T
ENST00000567159.5:c.1138A>T	ENSP00000456489.1:p.Lys380Ter
ENST00000567411.5:c.*659A>T	ENSP00000455545.1:n.*659A>T
ENST00000568777.5:n.6542A>T
ENST00000569410.5:c.1073+354A>T	ENSP00000457125.1:n.1073+354A>T
NM_000520.4:c.1138A>T	NP_000511.2:p.Lys380Ter
NM_000520.5:c.1138A>T	NP_000511.2:p.Lys380Ter
NM_001318825.1:c.1171A>T	NP_001305754.1:p.Lys391Ter
NR_134869.1:n.1574+354A>T
NM_000520.6:c.1138A>T MANE Select	NP_000511.2:p.Lys380Ter
NM_001318825.2:c.1171A>T	NP_001305754.1:p.Lys391Ter
NR_134869.2:n.1115+354A>T
NR_134869.3:n.1115+354A>T