Canonical Allele Identifier: CA2629339587

Gene: HEXA

Linked Data

• gnomAD v4: 15-72343553-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72343553G>T , CM000677.2:g.72343553G>T	GRCh38
NC_000015.9:g.72635894G>T , CM000677.1:g.72635894G>T	GRCh37
NC_000015.8:g.70422948G>T	NCBI36
NG_009017.1:g.37627C>A
NG_009017.2:g.37627C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682064.1:n.2341C>A
ENST00000682235.1:n.2137C>A
ENST00000682461.1:c.2220C>A	ENSP00000507308.1:n.2220C>A
ENST00000682653.1:n.4423C>A
ENST00000682721.1:c.*1917C>A	ENSP00000507535.1:n.*1917C>A
ENST00000682843.1:c.*1755C>A	ENSP00000508173.1:n.*1755C>A
ENST00000683133.1:c.2298C>A	ENSP00000508108.1:n.2298C>A
ENST00000683243.1:c.*1267C>A	ENSP00000507042.1:n.*1267C>A
ENST00000683463.1:c.*1603C>A	ENSP00000507986.1:n.*1603C>A
ENST00000683548.1:n.2572C>A
ENST00000683579.1:c.*2012C>A	ENSP00000506867.1:n.*2012C>A
ENST00000683587.1:n.2645C>A
ENST00000683735.1:c.*2512C>A	ENSP00000508336.1:n.*2512C>A
ENST00000683853.1:c.*2224C>A	ENSP00000506834.1:n.*2224C>A
ENST00000684125.1:c.*774C>A	ENSP00000507320.1:n.*774C>A
ENST00000684203.1:n.4563C>A
ENST00000684231.1:c.*1524C>A	ENSP00000507748.1:n.*1524C>A
ENST00000684263.1:c.*1738C>A	ENSP00000508369.1:n.*1738C>A
ENST00000684305.1:c.2562C>A	ENSP00000506819.1:n.2562C>A
ENST00000684602.1:c.*1780C>A	ENSP00000507996.1:n.*1780C>A
ENST00000684667.1:c.2445C>A	ENSP00000507003.1:n.2445C>A
ENST00000268097.10:c.*524C>A MANE Select	ENSP00000268097.6:n.*524C>A
ENST00000268097.9:c.*524C>A	ENSP00000268097.5:n.*524C>A
ENST00000379915.4:c.608+1893C>A	ENSP00000478716.1:n.608+1893C>A
NM_000520.4:c.*524C>A	NP_000511.2:n.*524C>A
NM_000520.5:c.*524C>A	NP_000511.2:n.*524C>A
NM_001318825.1:c.*524C>A	NP_001305754.1:n.*524C>A
NM_000520.6:c.*524C>A MANE Select	NP_000511.2:n.*524C>A
NM_001318825.2:c.*524C>A	NP_001305754.1:n.*524C>A