Canonical Allele Identifier: CA2186744394

Gene: HEXA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72348009_72348010delinsAC , CM000677.2:g.72348009_72348010delinsAC	GRCh38
NC_000015.9:g.72640350_72640351delinsAC , CM000677.1:g.72640350_72640351delinsAC	GRCh37
NC_000015.8:g.70427404_70427405delinsAC	NCBI36
NG_009017.1:g.33170_33171delinsGT
NG_009017.2:g.33170_33171delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563908.2:n.3457_3458delinsGT
ENST00000567027.6:c.1073+38_1073+39delinsGT	ENSP00000457521.2:n.1073+38_1073+39delinsGT
ENST00000682061.1:c.*735+38_*735+39delinsGT	ENSP00000508316.1:n.*735+38_*735+39delinsGT
ENST00000682177.1:c.1116+38_1116+39delinsGT	ENSP00000507409.1:n.1116+38_1116+39delinsGT
ENST00000682461.1:c.1179+38_1179+39delinsGT	ENSP00000507308.1:n.1179+38_1179+39delinsGT
ENST00000682653.1:n.1142_1143delinsGT
ENST00000682657.1:c.*483+38_*483+39delinsGT	ENSP00000507753.1:n.*483+38_*483+39delinsGT
ENST00000682721.1:c.*876+38_*876+39delinsGT	ENSP00000507535.1:n.*876+38_*876+39delinsGT
ENST00000682843.1:c.*971+38_*971+39delinsGT	ENSP00000508173.1:n.*971+38_*971+39delinsGT
ENST00000683003.1:c.*483+38_*483+39delinsGT	ENSP00000507576.1:n.*483+38_*483+39delinsGT
ENST00000683133.1:c.1257+38_1257+39delinsGT	ENSP00000508108.1:n.1257+38_1257+39delinsGT
ENST00000683228.1:n.1104+38_1104+39delinsGT
ENST00000683243.1:c.*483+38_*483+39delinsGT	ENSP00000507042.1:n.*483+38_*483+39delinsGT
ENST00000683463.1:c.1073+38_1073+39delinsGT	ENSP00000507986.1:n.1073+38_1073+39delinsGT
ENST00000683548.1:n.1104+38_1104+39delinsGT
ENST00000683579.1:c.*971+38_*971+39delinsGT	ENSP00000506867.1:n.*971+38_*971+39delinsGT
ENST00000683587.1:n.1104+38_1104+39delinsGT
ENST00000683681.1:c.1073+38_1073+39delinsGT	ENSP00000508110.1:n.1073+38_1073+39delinsGT
ENST00000683735.1:c.*971+38_*971+39delinsGT	ENSP00000508336.1:n.*971+38_*971+39delinsGT
ENST00000683742.1:n.904+38_904+39delinsGT
ENST00000683853.1:c.1073+38_1073+39delinsGT	ENSP00000506834.1:n.1073+38_1073+39delinsGT
ENST00000683860.1:c.1073+38_1073+39delinsGT	ENSP00000507179.1:n.1073+38_1073+39delinsGT
ENST00000683884.1:c.1073+38_1073+39delinsGT	ENSP00000507004.1:n.1073+38_1073+39delinsGT
ENST00000684041.1:c.1073+38_1073+39delinsGT	ENSP00000508382.1:n.1073+38_1073+39delinsGT
ENST00000684125.1:c.1073+38_1073+39delinsGT	ENSP00000507320.1:n.1073+38_1073+39delinsGT
ENST00000684203.1:n.2911+38_2911+39delinsGT
ENST00000684231.1:c.*483+38_*483+39delinsGT	ENSP00000507748.1:n.*483+38_*483+39delinsGT
ENST00000684263.1:c.*13+21_*13+22delinsGT	ENSP00000508369.1:n.*13+21_*13+22delinsGT
ENST00000684305.1:c.1521+38_1521+39delinsGT	ENSP00000506819.1:n.1521+38_1521+39delinsGT
ENST00000684415.1:c.*13+21_*13+22delinsGT	ENSP00000507227.1:n.*13+21_*13+22delinsGT
ENST00000684520.1:c.1073+38_1073+39delinsGT	ENSP00000506826.1:n.1073+38_1073+39delinsGT
ENST00000684602.1:c.*739+38_*739+39delinsGT	ENSP00000507996.1:n.*739+38_*739+39delinsGT
ENST00000684667.1:c.1404+38_1404+39delinsGT	ENSP00000507003.1:n.1404+38_1404+39delinsGT
ENST00000268097.10:c.1073+38_1073+39delinsGT MANE Select	ENSP00000268097.6:n.1073+38_1073+39delinsGT
ENST00000268097.9:c.1073+38_1073+39delinsGT	ENSP00000268097.5:n.1073+38_1073+39delinsGT
ENST00000379915.4:c.413-1685_413-1684delinsGT	ENSP00000478716.1:n.413-1685_413-1684delinsGT
ENST00000563762.5:c.825+38_825+39delinsGT	ENSP00000456346.1:n.825+38_825+39delinsGT
ENST00000566304.5:c.1106+38_1106+39delinsGT	ENSP00000455114.1:n.1106+38_1106+39delinsGT
ENST00000566672.5:c.*483+38_*483+39delinsGT	ENSP00000457037.1:n.*483+38_*483+39delinsGT
ENST00000567027.5:c.945+38_945+39delinsGT
ENST00000567159.5:c.1073+38_1073+39delinsGT	ENSP00000456489.1:n.1073+38_1073+39delinsGT
ENST00000567411.5:c.*594+38_*594+39delinsGT	ENSP00000455545.1:n.*594+38_*594+39delinsGT
ENST00000568777.5:n.6477+38_6477+39delinsGT
ENST00000569410.5:c.1073+38_1073+39delinsGT	ENSP00000457125.1:n.1073+38_1073+39delinsGT
NM_000520.4:c.1073+38_1073+39delinsGT	NP_000511.2:n.1073+38_1073+39delinsGT
NM_000520.5:c.1073+38_1073+39delinsGT	NP_000511.2:n.1073+38_1073+39delinsGT
NM_001318825.1:c.1106+38_1106+39delinsGT	NP_001305754.1:n.1106+38_1106+39delinsGT
NR_134869.1:n.1574+38_1574+39delinsGT
NM_000520.6:c.1073+38_1073+39delinsGT MANE Select	NP_000511.2:n.1073+38_1073+39delinsGT
NM_001318825.2:c.1106+38_1106+39delinsGT	NP_001305754.1:n.1106+38_1106+39delinsGT
NR_134869.2:n.1115+38_1115+39delinsGT
NR_134869.3:n.1115+38_1115+39delinsGT