Canonical Allele Identifier: CA618961257

Gene: HEXA

Linked Data

• dbSNP Id: rs1283877260
• gnomAD v2: 15-72637741-TG-T
• gnomAD v4: 15-72345400-TG-T
• MyVariant Identifiers: chr15:g.72637742del (hg19) ; chr15:g.72345401del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72345402del , CM000677.2:g.72345402del	GRCh38
NC_000015.9:g.72637743del , CM000677.1:g.72637743del	GRCh37
NC_000015.8:g.70424797del	NCBI36
NG_009017.1:g.35779del
NG_009017.2:g.35779del

Transcript Alleles

HGVS	Amino-acid change
ENST00000567027.6:c.*231del	ENSP00000457521.2:n.*231del
ENST00000682061.1:c.*1917del	ENSP00000508316.1:n.*1917del
ENST00000682064.1:n.1753+45del
ENST00000682177.1:c.1614del	ENSP00000507409.1:n.1614del
ENST00000682235.1:n.1549+45del
ENST00000682461.1:c.1632+45del	ENSP00000507308.1:n.1632+45del
ENST00000682653.1:n.2575del
ENST00000682657.1:c.*1408del	ENSP00000507753.1:n.*1408del
ENST00000682721.1:c.*1329+45del	ENSP00000507535.1:n.*1329+45del
ENST00000682843.1:c.*1167+45del	ENSP00000508173.1:n.*1167+45del
ENST00000683003.1:c.*1408del	ENSP00000507576.1:n.*1408del
ENST00000683133.1:c.1710+45del	ENSP00000508108.1:n.1710+45del
ENST00000683243.1:c.*679+45del	ENSP00000507042.1:n.*679+45del
ENST00000683463.1:c.*1015+45del	ENSP00000507986.1:n.*1015+45del
ENST00000683548.1:n.1984+45del
ENST00000683579.1:c.*1424+45del	ENSP00000506867.1:n.*1424+45del
ENST00000683587.1:n.2057+45del
ENST00000683681.1:c.*204+45del	ENSP00000508110.1:n.*204+45del
ENST00000683735.1:c.*1924+45del	ENSP00000508336.1:n.*1924+45del
ENST00000683853.1:c.*376del	ENSP00000506834.1:n.*376del
ENST00000683860.1:c.*646+45del	ENSP00000507179.1:n.*646+45del
ENST00000683884.1:c.*898del	ENSP00000507004.1:n.*898del
ENST00000684125.1:c.*186+45del	ENSP00000507320.1:n.*186+45del
ENST00000684203.1:n.3975+45del
ENST00000684231.1:c.*936+45del	ENSP00000507748.1:n.*936+45del
ENST00000684263.1:c.*1150+45del	ENSP00000508369.1:n.*1150+45del
ENST00000684305.1:c.1974+45del	ENSP00000506819.1:n.1974+45del
ENST00000684415.1:c.*1122del	ENSP00000507227.1:n.*1122del
ENST00000684520.1:c.*830del	ENSP00000506826.1:n.*830del
ENST00000684602.1:c.*1192+45del	ENSP00000507996.1:n.*1192+45del
ENST00000684667.1:c.1857+45del	ENSP00000507003.1:n.1857+45del
ENST00000268097.10:c.1526+45del MANE Select	ENSP00000268097.6:n.1526+45del
ENST00000268097.9:c.1526+45del	ENSP00000268097.5:n.1526+45del
ENST00000379915.4:c.608+45del	ENSP00000478716.1:n.608+45del
ENST00000564677.5:n.318+45del
ENST00000565873.1:n.437+45del
ENST00000566304.5:c.1559+45del	ENSP00000455114.1:n.1559+45del
ENST00000567027.5:c.1186del
ENST00000567411.5:c.*1047+45del	ENSP00000455545.1:n.*1047+45del
ENST00000568777.5:n.6791del
ENST00000569116.1:n.278del
NM_000520.4:c.1526+45del	NP_000511.2:n.1526+45del
NM_000520.5:c.1526+45del	NP_000511.2:n.1526+45del
NM_001318825.1:c.1559+45del	NP_001305754.1:n.1559+45del
NR_134869.1:n.1815del
NM_000520.6:c.1526+45del MANE Select	NP_000511.2:n.1526+45del
NM_001318825.2:c.1559+45del	NP_001305754.1:n.1559+45del
NR_134869.2:n.1356del
NR_134869.3:n.1356del