Canonical Allele Identifier: CA393062989

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72642862G>A (hg19) ; chr15:g.72350521G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72350521G>A , CM000677.2:g.72350521G>A	GRCh38
NC_000015.9:g.72642862G>A , CM000677.1:g.72642862G>A	GRCh37
NC_000015.8:g.70429916G>A	NCBI36
NG_009017.1:g.30659C>T
NG_009017.2:g.30659C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000563908.2:n.3148C>T
ENST00000567027.6:c.802C>T	ENSP00000457521.2:p.Pro268Ser
ENST00000682061.1:c.*464C>T	ENSP00000508316.1:n.*464C>T
ENST00000682177.1:c.845C>T	ENSP00000507409.1:n.845C>T
ENST00000682461.1:c.908C>T	ENSP00000507308.1:n.908C>T
ENST00000682653.1:n.833C>T
ENST00000682657.1:c.*212C>T	ENSP00000507753.1:n.*212C>T
ENST00000682721.1:c.*605C>T	ENSP00000507535.1:n.*605C>T
ENST00000682843.1:c.*700C>T	ENSP00000508173.1:n.*700C>T
ENST00000683003.1:c.*212C>T	ENSP00000507576.1:n.*212C>T
ENST00000683133.1:c.986C>T	ENSP00000508108.1:n.986C>T
ENST00000683228.1:n.833C>T
ENST00000683243.1:c.*212C>T	ENSP00000507042.1:n.*212C>T
ENST00000683463.1:c.802C>T	ENSP00000507986.1:p.Pro268Ser
ENST00000683548.1:n.833C>T
ENST00000683579.1:c.*700C>T	ENSP00000506867.1:n.*700C>T
ENST00000683587.1:n.833C>T
ENST00000683681.1:c.802C>T	ENSP00000508110.1:p.Pro268Ser
ENST00000683735.1:c.*700C>T	ENSP00000508336.1:n.*700C>T
ENST00000683742.1:n.633C>T
ENST00000683853.1:c.802C>T	ENSP00000506834.1:p.Pro268Ser
ENST00000683860.1:c.802C>T	ENSP00000507179.1:p.Pro268Ser
ENST00000683884.1:c.802C>T	ENSP00000507004.1:p.Pro268Ser
ENST00000684041.1:c.802C>T	ENSP00000508382.1:p.Pro268Ser
ENST00000684125.1:c.802C>T	ENSP00000507320.1:p.Pro268Ser
ENST00000684203.1:n.2640C>T
ENST00000684231.1:c.*212C>T	ENSP00000507748.1:n.*212C>T
ENST00000684263.1:c.802C>T	ENSP00000508369.1:p.Pro268Ser
ENST00000684305.1:c.1250C>T	ENSP00000506819.1:n.1250C>T
ENST00000684415.1:c.802C>T	ENSP00000507227.1:p.Pro268Ser
ENST00000684520.1:c.802C>T	ENSP00000506826.1:p.Pro268Ser
ENST00000684602.1:c.*468C>T	ENSP00000507996.1:n.*468C>T
ENST00000684667.1:c.1133C>T	ENSP00000507003.1:n.1133C>T
ENST00000268097.10:c.802C>T MANE Select	ENSP00000268097.6:p.Pro268Ser
ENST00000268097.9:c.802C>T	ENSP00000268097.5:p.Pro268Ser
ENST00000379915.4:c.413-4196C>T	ENSP00000478716.1:n.413-4196C>T
ENST00000563762.5:c.735C>T	ENSP00000456346.1:n.735C>T
ENST00000566304.5:c.835C>T	ENSP00000455114.1:p.Pro279Ser
ENST00000566672.5:c.*212C>T	ENSP00000457037.1:n.*212C>T
ENST00000567027.5:c.674C>T
ENST00000567159.5:c.802C>T	ENSP00000456489.1:p.Pro268Ser
ENST00000567411.5:c.*323C>T	ENSP00000455545.1:n.*323C>T
ENST00000568777.5:n.6206C>T
ENST00000569410.5:c.802C>T	ENSP00000457125.1:p.Pro268Ser
NM_000520.4:c.802C>T	NP_000511.2:p.Pro268Ser
NM_000520.5:c.802C>T	NP_000511.2:p.Pro268Ser
NM_001318825.1:c.835C>T	NP_001305754.1:p.Pro279Ser
NR_134869.1:n.1303C>T
NM_000520.6:c.802C>T MANE Select	NP_000511.2:p.Pro268Ser
NM_001318825.2:c.835C>T	NP_001305754.1:p.Pro279Ser
NR_134869.2:n.844C>T
NR_134869.3:n.844C>T