Canonical Allele Identifier: CA7644666

Gene: HEXA

Linked Data

• ClinVar Variation Id: 2139666
• ClinVar RCV Id: RCV003066651 ; RCV003066652 ; RCV003481372
• dbSNP Id: rs373781108
• ExAC: 15:72637826 G / C
• gnomAD v2: 15-72637826-G-C
• gnomAD v3: 15-72345485-G-C
• gnomAD v4: 15-72345485-G-C
• MyVariant Identifiers: chr15:g.72637826G>C (hg19) ; chr15:g.72345485G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345485G>C , CM000677.2:g.72345485G>C	GRCh38
NC_000015.9:g.72637826G>C , CM000677.1:g.72637826G>C	GRCh37
NC_000015.8:g.70424880G>C	NCBI36
NG_009017.1:g.35695C>G
NG_009017.2:g.35695C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000567027.6:c.*147C>G	ENSP00000457521.2:n.*147C>G
ENST00000682061.1:c.*1833C>G	ENSP00000508316.1:n.*1833C>G
ENST00000682064.1:n.1714C>G
ENST00000682177.1:c.1530C>G	ENSP00000507409.1:n.1530C>G
ENST00000682235.1:n.1510C>G
ENST00000682461.1:c.1593C>G	ENSP00000507308.1:n.1593C>G
ENST00000682653.1:n.2491C>G
ENST00000682657.1:c.*1324C>G	ENSP00000507753.1:n.*1324C>G
ENST00000682721.1:c.*1290C>G	ENSP00000507535.1:n.*1290C>G
ENST00000682843.1:c.*1128C>G	ENSP00000508173.1:n.*1128C>G
ENST00000683003.1:c.*1324C>G	ENSP00000507576.1:n.*1324C>G
ENST00000683133.1:c.1671C>G	ENSP00000508108.1:n.1671C>G
ENST00000683243.1:c.*640C>G	ENSP00000507042.1:n.*640C>G
ENST00000683463.1:c.*976C>G	ENSP00000507986.1:n.*976C>G
ENST00000683548.1:n.1945C>G
ENST00000683579.1:c.*1385C>G	ENSP00000506867.1:n.*1385C>G
ENST00000683587.1:n.2018C>G
ENST00000683681.1:c.*165C>G	ENSP00000508110.1:n.*165C>G
ENST00000683735.1:c.*1885C>G	ENSP00000508336.1:n.*1885C>G
ENST00000683853.1:c.*292C>G	ENSP00000506834.1:n.*292C>G
ENST00000683860.1:c.*607C>G	ENSP00000507179.1:n.*607C>G
ENST00000683884.1:c.*814C>G	ENSP00000507004.1:n.*814C>G
ENST00000684041.1:c.*620C>G	ENSP00000508382.1:n.*620C>G
ENST00000684125.1:c.*147C>G	ENSP00000507320.1:n.*147C>G
ENST00000684203.1:n.3936C>G
ENST00000684231.1:c.*897C>G	ENSP00000507748.1:n.*897C>G
ENST00000684263.1:c.*1111C>G	ENSP00000508369.1:n.*1111C>G
ENST00000684305.1:c.1935C>G	ENSP00000506819.1:n.1935C>G
ENST00000684415.1:c.*1038C>G	ENSP00000507227.1:n.*1038C>G
ENST00000684520.1:c.*746C>G	ENSP00000506826.1:n.*746C>G
ENST00000684602.1:c.*1153C>G	ENSP00000507996.1:n.*1153C>G
ENST00000684667.1:c.1818C>G	ENSP00000507003.1:n.1818C>G
ENST00000268097.10:c.1487C>G MANE Select	ENSP00000268097.6:p.Ala496Gly
ENST00000268097.9:c.1487C>G	ENSP00000268097.5:p.Ala496Gly
ENST00000379915.4:c.569C>G	ENSP00000478716.1:p.Ala190Gly
ENST00000564677.5:n.279C>G
ENST00000565873.1:n.398C>G
ENST00000566304.5:c.1520C>G	ENSP00000455114.1:p.Ala507Gly
ENST00000567027.5:c.1102C>G
ENST00000567159.5:c.1487C>G	ENSP00000456489.1:p.Ala496Gly
ENST00000567411.5:c.*1008C>G	ENSP00000455545.1:n.*1008C>G
ENST00000568777.5:n.6707C>G
ENST00000569116.1:n.194C>G
NM_000520.4:c.1487C>G	NP_000511.2:p.Ala496Gly
NM_000520.5:c.1487C>G	NP_000511.2:p.Ala496Gly
NM_001318825.1:c.1520C>G	NP_001305754.1:p.Ala507Gly
NR_134869.1:n.1731C>G
NM_000520.6:c.1487C>G MANE Select	NP_000511.2:p.Ala496Gly
NM_001318825.2:c.1520C>G	NP_001305754.1:p.Ala507Gly
NR_134869.2:n.1272C>G
NR_134869.3:n.1272C>G