Canonical Allele Identifier: CA7645007

Gene: HEXA

Linked Data

• dbSNP Id: rs750784687
• ExAC: 15:72646035 G / A
• gnomAD v2: 15-72646035-G-A
• MyVariant Identifiers: chr15:g.72646035G>A (hg19) ; chr15:g.72353694G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72353694G>A , CM000677.2:g.72353694G>A	GRCh38
NC_000015.9:g.72646035G>A , CM000677.1:g.72646035G>A	GRCh37
NC_000015.8:g.70433089G>A	NCBI36
NG_009017.1:g.27486C>T
NG_009017.2:g.27486C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000563908.2:n.2290C>T
ENST00000567027.6:c.456C>T	ENSP00000457521.2:p.Gly152=
ENST00000568260.2:c.480-516C>T	ENSP00000458128.2:n.480-516C>T
ENST00000682061.1:c.*118C>T	ENSP00000508316.1:n.*118C>T
ENST00000682177.1:c.456C>T	ENSP00000507409.1:p.Gly152=
ENST00000682461.1:c.676+1865C>T	ENSP00000507308.1:n.676+1865C>T
ENST00000682653.1:n.487C>T
ENST00000682657.1:c.254-2460C>T	ENSP00000507753.1:n.254-2460C>T
ENST00000682721.1:c.*259C>T	ENSP00000507535.1:n.*259C>T
ENST00000682843.1:c.*354C>T	ENSP00000508173.1:n.*354C>T
ENST00000683003.1:c.412+1865C>T	ENSP00000507576.1:n.412+1865C>T
ENST00000683133.1:c.640C>T	ENSP00000508108.1:n.640C>T
ENST00000683228.1:n.487C>T
ENST00000683243.1:c.412+1865C>T	ENSP00000507042.1:n.412+1865C>T
ENST00000683463.1:c.456C>T	ENSP00000507986.1:p.Gly152=
ENST00000683548.1:n.487C>T
ENST00000683579.1:c.*354C>T	ENSP00000506867.1:n.*354C>T
ENST00000683587.1:n.487C>T
ENST00000683681.1:c.456C>T	ENSP00000508110.1:p.Gly152=
ENST00000683735.1:c.*354C>T	ENSP00000508336.1:n.*354C>T
ENST00000683853.1:c.456C>T	ENSP00000506834.1:p.Gly152=
ENST00000683860.1:c.456C>T	ENSP00000507179.1:p.Gly152=
ENST00000683884.1:c.456C>T	ENSP00000507004.1:p.Gly152=
ENST00000684041.1:c.456C>T	ENSP00000508382.1:p.Gly152=
ENST00000684125.1:c.456C>T	ENSP00000507320.1:p.Gly152=
ENST00000684203.1:n.2294C>T
ENST00000684231.1:c.412+1865C>T	ENSP00000507748.1:n.412+1865C>T
ENST00000684263.1:c.456C>T	ENSP00000508369.1:p.Gly152=
ENST00000684305.1:c.904C>T	ENSP00000506819.1:n.904C>T
ENST00000684415.1:c.456C>T	ENSP00000507227.1:p.Gly152=
ENST00000684520.1:c.456C>T	ENSP00000506826.1:p.Gly152=
ENST00000684602.1:c.*236+1865C>T	ENSP00000507996.1:n.*236+1865C>T
ENST00000684667.1:c.787C>T	ENSP00000507003.1:n.787C>T
ENST00000268097.10:c.456C>T MANE Select	ENSP00000268097.6:p.Gly152=
ENST00000268097.9:c.456C>T	ENSP00000268097.5:p.Gly152=
ENST00000379915.4:c.412+1865C>T	ENSP00000478716.1:n.412+1865C>T
ENST00000563762.5:c.503+1865C>T	ENSP00000456346.1:n.503+1865C>T
ENST00000566304.5:c.489C>T	ENSP00000455114.1:p.Gly163=
ENST00000566672.5:c.412+1865C>T	ENSP00000457037.1:n.412+1865C>T
ENST00000567027.5:c.328C>T
ENST00000567159.5:c.456C>T	ENSP00000456489.1:p.Gly152=
ENST00000567411.5:c.413-516C>T	ENSP00000455545.1:n.413-516C>T
ENST00000568260.1:c.461-516C>T
ENST00000568777.5:n.5860C>T
ENST00000569410.5:c.456C>T	ENSP00000457125.1:p.Gly152=
ENST00000569509.5:n.417+1865C>T
NM_000520.4:c.456C>T	NP_000511.2:p.Gly152=
NM_000520.5:c.456C>T	NP_000511.2:p.Gly152=
NM_001318825.1:c.489C>T	NP_001305754.1:p.Gly163=
NR_134869.1:n.957C>T
NM_000520.6:c.456C>T MANE Select	NP_000511.2:p.Gly152=
NM_001318825.2:c.489C>T	NP_001305754.1:p.Gly163=
NR_134869.2:n.498C>T
NR_134869.3:n.498C>T