Canonical Allele Identifier: CA272631599
Gene: HEXA HGNC NCBI

Linked Data

dbSNP Id: rs1020840083

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72376066dup , CM000677.2:g.72376066dup GRCh38
NC_000015.9:g.72668407dup , CM000677.1:g.72668407dup GRCh37
NC_000015.8:g.70455461dup NCBI36
NG_009017.1:g.5115dup
NG_009017.2:g.5115dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000268097.9:c.-93dup ENSP00000268097.5:n.-93dup
ENST00000569509.5:n.146+210dup
NM_000520.4:c.-93dup NP_000511.2:n.-93dup
NM_000520.5:c.-93dup NP_000511.2:n.-93dup
NM_001318825.1:c.-93dup NP_001305754.1:n.-93dup
NR_134869.1:n.409dup