Canonical Allele Identifier: CA715470352

Gene: HEXA

Linked Data

• dbSNP Id: rs1487922326
• gnomAD v3: 15-72345098-A-G
• gnomAD v4: 15-72345098-A-G
• MyVariant Identifiers: chr15:g.72637439A>G (hg19) ; chr15:g.72345098A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345098A>G , CM000677.2:g.72345098A>G	GRCh38
NC_000015.9:g.72637439A>G , CM000677.1:g.72637439A>G	GRCh37
NC_000015.8:g.70424493A>G	NCBI36
NG_009017.1:g.36082T>C
NG_009017.2:g.36082T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682064.1:n.1753+348T>C
ENST00000682235.1:n.1549+348T>C
ENST00000682461.1:c.1632+348T>C	ENSP00000507308.1:n.1632+348T>C
ENST00000682653.1:n.2878T>C
ENST00000682721.1:c.*1329+348T>C	ENSP00000507535.1:n.*1329+348T>C
ENST00000682843.1:c.*1167+348T>C	ENSP00000508173.1:n.*1167+348T>C
ENST00000683133.1:c.1710+348T>C	ENSP00000508108.1:n.1710+348T>C
ENST00000683243.1:c.*679+348T>C	ENSP00000507042.1:n.*679+348T>C
ENST00000683463.1:c.*1015+348T>C	ENSP00000507986.1:n.*1015+348T>C
ENST00000683548.1:n.1984+348T>C
ENST00000683579.1:c.*1424+348T>C	ENSP00000506867.1:n.*1424+348T>C
ENST00000683587.1:n.2057+348T>C
ENST00000683681.1:c.*204+348T>C	ENSP00000508110.1:n.*204+348T>C
ENST00000683735.1:c.*1924+348T>C	ENSP00000508336.1:n.*1924+348T>C
ENST00000683853.1:c.*679T>C	ENSP00000506834.1:n.*679T>C
ENST00000683860.1:c.*646+348T>C	ENSP00000507179.1:n.*646+348T>C
ENST00000684125.1:c.*186+348T>C	ENSP00000507320.1:n.*186+348T>C
ENST00000684203.1:n.3975+348T>C
ENST00000684231.1:c.*936+348T>C	ENSP00000507748.1:n.*936+348T>C
ENST00000684263.1:c.*1150+348T>C	ENSP00000508369.1:n.*1150+348T>C
ENST00000684305.1:c.1974+348T>C	ENSP00000506819.1:n.1974+348T>C
ENST00000684602.1:c.*1192+348T>C	ENSP00000507996.1:n.*1192+348T>C
ENST00000684667.1:c.1857+348T>C	ENSP00000507003.1:n.1857+348T>C
ENST00000268097.10:c.1526+348T>C MANE Select	ENSP00000268097.6:n.1526+348T>C
ENST00000268097.9:c.1526+348T>C	ENSP00000268097.5:n.1526+348T>C
ENST00000379915.4:c.608+348T>C	ENSP00000478716.1:n.608+348T>C
ENST00000564677.5:n.318+348T>C
ENST00000565873.1:n.437+348T>C
ENST00000566304.5:c.1559+348T>C	ENSP00000455114.1:n.1559+348T>C
ENST00000567411.5:c.*1047+348T>C	ENSP00000455545.1:n.*1047+348T>C
NM_000520.4:c.1526+348T>C	NP_000511.2:n.1526+348T>C
NM_000520.5:c.1526+348T>C	NP_000511.2:n.1526+348T>C
NM_001318825.1:c.1559+348T>C	NP_001305754.1:n.1559+348T>C
NM_000520.6:c.1526+348T>C MANE Select	NP_000511.2:n.1526+348T>C
NM_001318825.2:c.1559+348T>C	NP_001305754.1:n.1559+348T>C