Canonical Allele Identifier: CA491121306

Gene: HEXA

Linked Data

• MyVariant Identifiers: chr15:g.72642780A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72350439A>C , CM000677.2:g.72350439A>C	GRCh38
NC_000015.9:g.72642780A>C , CM000677.1:g.72642780A>C	GRCh37
NC_000015.8:g.70429834A>C	NCBI36
NG_009017.1:g.30741T>G
NG_009017.2:g.30741T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000563908.2:n.3151+79T>G
ENST00000567027.6:c.805+79T>G	ENSP00000457521.2:n.805+79T>G
ENST00000682061.1:c.*467+79T>G	ENSP00000508316.1:n.*467+79T>G
ENST00000682177.1:c.848+79T>G	ENSP00000507409.1:n.848+79T>G
ENST00000682461.1:c.911+79T>G	ENSP00000507308.1:n.911+79T>G
ENST00000682653.1:n.836+79T>G
ENST00000682657.1:c.*215+79T>G	ENSP00000507753.1:n.*215+79T>G
ENST00000682721.1:c.*608+79T>G	ENSP00000507535.1:n.*608+79T>G
ENST00000682843.1:c.*703+79T>G	ENSP00000508173.1:n.*703+79T>G
ENST00000683003.1:c.*215+79T>G	ENSP00000507576.1:n.*215+79T>G
ENST00000683133.1:c.989+79T>G	ENSP00000508108.1:n.989+79T>G
ENST00000683228.1:n.836+79T>G
ENST00000683243.1:c.*215+79T>G	ENSP00000507042.1:n.*215+79T>G
ENST00000683463.1:c.805+79T>G	ENSP00000507986.1:n.805+79T>G
ENST00000683548.1:n.836+79T>G
ENST00000683579.1:c.*703+79T>G	ENSP00000506867.1:n.*703+79T>G
ENST00000683587.1:n.836+79T>G
ENST00000683681.1:c.805+79T>G	ENSP00000508110.1:n.805+79T>G
ENST00000683735.1:c.*703+79T>G	ENSP00000508336.1:n.*703+79T>G
ENST00000683742.1:n.636+79T>G
ENST00000683853.1:c.805+79T>G	ENSP00000506834.1:n.805+79T>G
ENST00000683860.1:c.805+79T>G	ENSP00000507179.1:n.805+79T>G
ENST00000683884.1:c.805+79T>G	ENSP00000507004.1:n.805+79T>G
ENST00000684041.1:c.805+79T>G	ENSP00000508382.1:n.805+79T>G
ENST00000684125.1:c.805+79T>G	ENSP00000507320.1:n.805+79T>G
ENST00000684203.1:n.2643+79T>G
ENST00000684231.1:c.*215+79T>G	ENSP00000507748.1:n.*215+79T>G
ENST00000684263.1:c.805+79T>G	ENSP00000508369.1:n.805+79T>G
ENST00000684305.1:c.1253+79T>G	ENSP00000506819.1:n.1253+79T>G
ENST00000684415.1:c.805+79T>G	ENSP00000507227.1:n.805+79T>G
ENST00000684520.1:c.805+79T>G	ENSP00000506826.1:n.805+79T>G
ENST00000684602.1:c.*471+79T>G	ENSP00000507996.1:n.*471+79T>G
ENST00000684667.1:c.1136+79T>G	ENSP00000507003.1:n.1136+79T>G
ENST00000268097.10:c.805+79T>G MANE Select	ENSP00000268097.6:n.805+79T>G
ENST00000268097.9:c.805+79T>G	ENSP00000268097.5:n.805+79T>G
ENST00000379915.4:c.413-4114T>G	ENSP00000478716.1:n.413-4114T>G
ENST00000563762.5:c.738+79T>G	ENSP00000456346.1:n.738+79T>G
ENST00000566304.5:c.838+79T>G	ENSP00000455114.1:n.838+79T>G
ENST00000566672.5:c.*215+79T>G	ENSP00000457037.1:n.*215+79T>G
ENST00000567027.5:c.677+79T>G
ENST00000567159.5:c.805+79T>G	ENSP00000456489.1:n.805+79T>G
ENST00000567411.5:c.*326+79T>G	ENSP00000455545.1:n.*326+79T>G
ENST00000568777.5:n.6209+79T>G
ENST00000569410.5:c.805+79T>G	ENSP00000457125.1:n.805+79T>G
NM_000520.4:c.805+79T>G	NP_000511.2:n.805+79T>G
NM_000520.5:c.805+79T>G	NP_000511.2:n.805+79T>G
NM_001318825.1:c.838+79T>G	NP_001305754.1:n.838+79T>G
NR_134869.1:n.1306+79T>G
NM_000520.6:c.805+79T>G MANE Select	NP_000511.2:n.805+79T>G
NM_001318825.2:c.838+79T>G	NP_001305754.1:n.838+79T>G
NR_134869.2:n.847+79T>G
NR_134869.3:n.847+79T>G