Canonical Allele Identifier: CA393066653

Gene: HEXA

Linked Data

• dbSNP Id: rs1437253103
• gnomAD v2: 15-72647920-G-C
• gnomAD v4: 15-72355579-G-C
• MyVariant Identifiers: chr15:g.72647920G>C (hg19) ; chr15:g.72355579G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72355579G>C , CM000677.2:g.72355579G>C	GRCh38
NC_000015.9:g.72647920G>C , CM000677.1:g.72647920G>C	GRCh37
NC_000015.8:g.70434974G>C	NCBI36
NG_009017.1:g.25601C>G
NG_009017.2:g.25601C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563908.2:n.405C>G
ENST00000567027.6:c.392C>G	ENSP00000457521.2:p.Thr131Ser
ENST00000568260.2:c.459C>G	ENSP00000458128.2:n.459C>G
ENST00000682061.1:c.*54C>G	ENSP00000508316.1:n.*54C>G
ENST00000682177.1:c.392C>G	ENSP00000507409.1:p.Thr131Ser
ENST00000682461.1:c.656C>G	ENSP00000507308.1:n.656C>G
ENST00000682653.1:n.423C>G
ENST00000682657.1:c.254-4345C>G	ENSP00000507753.1:n.254-4345C>G
ENST00000682721.1:c.*195C>G	ENSP00000507535.1:n.*195C>G
ENST00000682843.1:c.*290C>G	ENSP00000508173.1:n.*290C>G
ENST00000683003.1:c.392C>G	ENSP00000507576.1:p.Thr131Ser
ENST00000683133.1:c.576C>G	ENSP00000508108.1:n.576C>G
ENST00000683228.1:n.423C>G
ENST00000683243.1:c.392C>G	ENSP00000507042.1:p.Thr131Ser
ENST00000683463.1:c.392C>G	ENSP00000507986.1:p.Thr131Ser
ENST00000683548.1:n.423C>G
ENST00000683579.1:c.*290C>G	ENSP00000506867.1:n.*290C>G
ENST00000683587.1:n.423C>G
ENST00000683681.1:c.392C>G	ENSP00000508110.1:p.Thr131Ser
ENST00000683735.1:c.*290C>G	ENSP00000508336.1:n.*290C>G
ENST00000683853.1:c.392C>G	ENSP00000506834.1:p.Thr131Ser
ENST00000683860.1:c.392C>G	ENSP00000507179.1:p.Thr131Ser
ENST00000683884.1:c.392C>G	ENSP00000507004.1:p.Thr131Ser
ENST00000684041.1:c.392C>G	ENSP00000508382.1:p.Thr131Ser
ENST00000684125.1:c.392C>G	ENSP00000507320.1:p.Thr131Ser
ENST00000684203.1:n.409C>G
ENST00000684231.1:c.392C>G	ENSP00000507748.1:p.Thr131Ser
ENST00000684263.1:c.392C>G	ENSP00000508369.1:p.Thr131Ser
ENST00000684305.1:c.840C>G	ENSP00000506819.1:n.840C>G
ENST00000684415.1:c.392C>G	ENSP00000507227.1:p.Thr131Ser
ENST00000684520.1:c.392C>G	ENSP00000506826.1:p.Thr131Ser
ENST00000684602.1:c.*216C>G	ENSP00000507996.1:n.*216C>G
ENST00000684667.1:c.723C>G	ENSP00000507003.1:n.723C>G
ENST00000268097.10:c.392C>G MANE Select	ENSP00000268097.6:p.Thr131Ser
ENST00000268097.9:c.392C>G	ENSP00000268097.5:p.Thr131Ser
ENST00000379915.4:c.392C>G	ENSP00000478716.1:p.Thr131Ser
ENST00000563762.5:c.483C>G	ENSP00000456346.1:n.483C>G
ENST00000563908.1:n.389C>G
ENST00000566304.5:c.425C>G	ENSP00000455114.1:p.Thr142Ser
ENST00000566672.5:c.392C>G	ENSP00000457037.1:p.Thr131Ser
ENST00000567027.5:c.264C>G
ENST00000567159.5:c.392C>G	ENSP00000456489.1:p.Thr131Ser
ENST00000567411.5:c.392C>G	ENSP00000455545.1:p.Thr131Ser
ENST00000568260.1:c.440C>G
ENST00000568777.5:n.3975C>G
ENST00000569410.5:c.392C>G	ENSP00000457125.1:p.Thr131Ser
ENST00000569509.5:n.397C>G
NM_000520.4:c.392C>G	NP_000511.2:p.Thr131Ser
NM_000520.5:c.392C>G	NP_000511.2:p.Thr131Ser
NM_001318825.1:c.425C>G	NP_001305754.1:p.Thr142Ser
NR_134869.1:n.893C>G
NM_000520.6:c.392C>G MANE Select	NP_000511.2:p.Thr131Ser
NM_001318825.2:c.425C>G	NP_001305754.1:p.Thr142Ser
NR_134869.2:n.434C>G
NR_134869.3:n.434C>G