Canonical Allele Identifier: CA2186761726
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72376036C= , CM000677.2:g.72376036C= GRCh38
NC_000015.9:g.72668377C= , CM000677.1:g.72668377C= GRCh37
NC_000015.8:g.70455431C= NCBI36
NG_009017.1:g.5144G=
NG_009017.2:g.5144G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268097.9:c.-64G= ENSP00000268097.5:n.-64G=
ENST00000569509.5:n.147-205G=
NM_000520.4:c.-64G= NP_000511.2:n.-64G=
NM_000520.5:c.-64G= NP_000511.2:n.-64G=
NM_001318825.1:c.-64G= NP_001305754.1:n.-64G=
NR_134869.1:n.438G=