Canonical Allele Identifier: CA7644943

Gene: HEXA

Linked Data

• ClinVar Variation Id: 2036932
• ClinVar RCV Id: RCV002882080
• dbSNP Id: rs762581234
• ExAC: 15:72643519 A / C
• gnomAD v2: 15-72643519-A-C
• gnomAD v4: 15-72351178-A-C
• MyVariant Identifiers: chr15:g.72643519A>C (hg19) ; chr15:g.72351178A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72351178A>C , CM000677.2:g.72351178A>C	GRCh38
NC_000015.9:g.72643519A>C , CM000677.1:g.72643519A>C	GRCh37
NC_000015.8:g.70430573A>C	NCBI36
NG_009017.1:g.30002T>G
NG_009017.2:g.30002T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563908.2:n.2973T>G
ENST00000567027.6:c.627T>G	ENSP00000457521.2:p.Pro209=
ENST00000568260.2:c.647T>G	ENSP00000458128.2:n.647T>G
ENST00000682061.1:c.*289T>G	ENSP00000508316.1:n.*289T>G
ENST00000682177.1:c.627T>G	ENSP00000507409.1:p.Pro209=
ENST00000682461.1:c.733T>G	ENSP00000507308.1:n.733T>G
ENST00000682653.1:n.658T>G
ENST00000682657.1:c.*37T>G	ENSP00000507753.1:n.*37T>G
ENST00000682721.1:c.*430T>G	ENSP00000507535.1:n.*430T>G
ENST00000682843.1:c.*525T>G	ENSP00000508173.1:n.*525T>G
ENST00000683003.1:c.*37T>G	ENSP00000507576.1:n.*37T>G
ENST00000683133.1:c.811T>G	ENSP00000508108.1:n.811T>G
ENST00000683228.1:n.658T>G
ENST00000683243.1:c.*37T>G	ENSP00000507042.1:n.*37T>G
ENST00000683463.1:c.627T>G	ENSP00000507986.1:p.Pro209=
ENST00000683548.1:n.658T>G
ENST00000683579.1:c.*525T>G	ENSP00000506867.1:n.*525T>G
ENST00000683587.1:n.658T>G
ENST00000683681.1:c.627T>G	ENSP00000508110.1:p.Pro209=
ENST00000683735.1:c.*525T>G	ENSP00000508336.1:n.*525T>G
ENST00000683742.1:n.458T>G
ENST00000683853.1:c.627T>G	ENSP00000506834.1:p.Pro209=
ENST00000683860.1:c.627T>G	ENSP00000507179.1:p.Pro209=
ENST00000683884.1:c.627T>G	ENSP00000507004.1:p.Pro209=
ENST00000684041.1:c.627T>G	ENSP00000508382.1:p.Pro209=
ENST00000684125.1:c.627T>G	ENSP00000507320.1:p.Pro209=
ENST00000684203.1:n.2465T>G
ENST00000684231.1:c.*37T>G	ENSP00000507748.1:n.*37T>G
ENST00000684263.1:c.627T>G	ENSP00000508369.1:p.Pro209=
ENST00000684305.1:c.1075T>G	ENSP00000506819.1:n.1075T>G
ENST00000684415.1:c.627T>G	ENSP00000507227.1:p.Pro209=
ENST00000684520.1:c.627T>G	ENSP00000506826.1:p.Pro209=
ENST00000684602.1:c.*293T>G	ENSP00000507996.1:n.*293T>G
ENST00000684667.1:c.958T>G	ENSP00000507003.1:n.958T>G
ENST00000268097.10:c.627T>G MANE Select	ENSP00000268097.6:p.Pro209=
ENST00000268097.9:c.627T>G	ENSP00000268097.5:p.Pro209=
ENST00000379915.4:c.412+4381T>G	ENSP00000478716.1:n.412+4381T>G
ENST00000563762.5:c.560T>G	ENSP00000456346.1:n.560T>G
ENST00000566304.5:c.660T>G	ENSP00000455114.1:p.Pro220=
ENST00000566672.5:c.*37T>G	ENSP00000457037.1:n.*37T>G
ENST00000567027.5:c.499T>G
ENST00000567159.5:c.627T>G	ENSP00000456489.1:p.Pro209=
ENST00000567411.5:c.*148T>G	ENSP00000455545.1:n.*148T>G
ENST00000568260.1:c.628T>G
ENST00000568777.5:n.6031T>G
ENST00000569410.5:c.627T>G	ENSP00000457125.1:p.Pro209=
ENST00000569509.5:n.474T>G
NM_000520.4:c.627T>G	NP_000511.2:p.Pro209=
NM_000520.5:c.627T>G	NP_000511.2:p.Pro209=
NM_001318825.1:c.660T>G	NP_001305754.1:p.Pro220=
NR_134869.1:n.1128T>G
NM_000520.6:c.627T>G MANE Select	NP_000511.2:p.Pro209=
NM_001318825.2:c.660T>G	NP_001305754.1:p.Pro220=
NR_134869.2:n.669T>G
NR_134869.3:n.669T>G