Canonical Allele Identifier: CA491119546

Gene: HEXA

Linked Data

• ClinVar Variation Id: 2757423
• ClinVar RCV Id: RCV003503123
• MyVariant Identifiers: chr15:g.72641470G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72349129G>A , CM000677.2:g.72349129G>A	GRCh38
NC_000015.9:g.72641470G>A , CM000677.1:g.72641470G>A	GRCh37
NC_000015.8:g.70428524G>A	NCBI36
NG_009017.1:g.32051C>T
NG_009017.2:g.32051C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563908.2:n.3282C>T
ENST00000567027.6:c.936C>T	ENSP00000457521.2:p.Phe312=
ENST00000682061.1:c.*598C>T	ENSP00000508316.1:n.*598C>T
ENST00000682177.1:c.979C>T	ENSP00000507409.1:n.979C>T
ENST00000682461.1:c.1042C>T	ENSP00000507308.1:n.1042C>T
ENST00000682653.1:n.967C>T
ENST00000682657.1:c.*346C>T	ENSP00000507753.1:n.*346C>T
ENST00000682721.1:c.*739C>T	ENSP00000507535.1:n.*739C>T
ENST00000682843.1:c.*834C>T	ENSP00000508173.1:n.*834C>T
ENST00000683003.1:c.*346C>T	ENSP00000507576.1:n.*346C>T
ENST00000683133.1:c.1120C>T	ENSP00000508108.1:n.1120C>T
ENST00000683228.1:n.967C>T
ENST00000683243.1:c.*346C>T	ENSP00000507042.1:n.*346C>T
ENST00000683463.1:c.936C>T	ENSP00000507986.1:p.Phe312=
ENST00000683548.1:n.967C>T
ENST00000683579.1:c.*834C>T	ENSP00000506867.1:n.*834C>T
ENST00000683587.1:n.967C>T
ENST00000683681.1:c.936C>T	ENSP00000508110.1:p.Phe312=
ENST00000683735.1:c.*834C>T	ENSP00000508336.1:n.*834C>T
ENST00000683742.1:n.767C>T
ENST00000683853.1:c.936C>T	ENSP00000506834.1:p.Phe312=
ENST00000683860.1:c.936C>T	ENSP00000507179.1:p.Phe312=
ENST00000683884.1:c.936C>T	ENSP00000507004.1:p.Phe312=
ENST00000684041.1:c.936C>T	ENSP00000508382.1:p.Phe312=
ENST00000684125.1:c.936C>T	ENSP00000507320.1:p.Phe312=
ENST00000684203.1:n.2774C>T
ENST00000684231.1:c.*346C>T	ENSP00000507748.1:n.*346C>T
ENST00000684263.1:c.936C>T	ENSP00000508369.1:p.Phe312=
ENST00000684305.1:c.1384C>T	ENSP00000506819.1:n.1384C>T
ENST00000684415.1:c.936C>T	ENSP00000507227.1:p.Phe312=
ENST00000684520.1:c.936C>T	ENSP00000506826.1:p.Phe312=
ENST00000684602.1:c.*602C>T	ENSP00000507996.1:n.*602C>T
ENST00000684667.1:c.1267C>T	ENSP00000507003.1:n.1267C>T
ENST00000268097.10:c.936C>T MANE Select	ENSP00000268097.6:p.Phe312=
ENST00000268097.9:c.936C>T	ENSP00000268097.5:p.Phe312=
ENST00000379915.4:c.413-2804C>T	ENSP00000478716.1:n.413-2804C>T
ENST00000563762.5:c.739-995C>T	ENSP00000456346.1:n.739-995C>T
ENST00000566304.5:c.969C>T	ENSP00000455114.1:p.Phe323=
ENST00000566672.5:c.*346C>T	ENSP00000457037.1:n.*346C>T
ENST00000567027.5:c.808C>T
ENST00000567159.5:c.936C>T	ENSP00000456489.1:p.Phe312=
ENST00000567411.5:c.*457C>T	ENSP00000455545.1:n.*457C>T
ENST00000568777.5:n.6340C>T
ENST00000569410.5:c.936C>T	ENSP00000457125.1:p.Phe312=
NM_000520.4:c.936C>T	NP_000511.2:p.Phe312=
NM_000520.5:c.936C>T	NP_000511.2:p.Phe312=
NM_001318825.1:c.969C>T	NP_001305754.1:p.Phe323=
NR_134869.1:n.1437C>T
NM_000520.6:c.936C>T MANE Select	NP_000511.2:p.Phe312=
NM_001318825.2:c.969C>T	NP_001305754.1:p.Phe323=
NR_134869.2:n.978C>T
NR_134869.3:n.978C>T