Canonical Allele Identifier: CA2186742349

Gene: HEXA

Linked Data

• dbSNP Id: rs2088572125

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72343451T>A , CM000677.2:g.72343451T>A	GRCh38
NC_000015.9:g.72635792T>A , CM000677.1:g.72635792T>A	GRCh37
NC_000015.8:g.70422846T>A	NCBI36
NG_009017.1:g.37729A>T
NG_009017.2:g.37729A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000683243.1:c.*1369A>T	ENSP00000507042.1:n.*1369A>T
ENST00000684263.1:c.*1840A>T	ENSP00000508369.1:n.*1840A>T
ENST00000268097.10:c.*626A>T MANE Select	ENSP00000268097.6:n.*626A>T
ENST00000268097.9:c.*626A>T	ENSP00000268097.5:n.*626A>T
ENST00000379915.4:c.608+1995A>T	ENSP00000478716.1:n.608+1995A>T
NM_000520.4:c.*626A>T	NP_000511.2:n.*626A>T
NM_000520.5:c.*626A>T	NP_000511.2:n.*626A>T
NM_001318825.1:c.*626A>T	NP_001305754.1:n.*626A>T
NM_000520.6:c.*626A>T MANE Select	NP_000511.2:n.*626A>T
NM_001318825.2:c.*626A>T	NP_001305754.1:n.*626A>T