Canonical Allele Identifier: CA2186761732
Gene: HEXA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72376040C= , CM000677.2:g.72376040C= GRCh38
NC_000015.9:g.72668381C= , CM000677.1:g.72668381C= GRCh37
NC_000015.8:g.70455435C= NCBI36
NG_009017.1:g.5140G=
NG_009017.2:g.5140G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268097.9:c.-68G= ENSP00000268097.5:n.-68G=
ENST00000569509.5:n.147-209G=
NM_000520.4:c.-68G= NP_000511.2:n.-68G=
NM_000520.5:c.-68G= NP_000511.2:n.-68G=
NM_001318825.1:c.-68G= NP_001305754.1:n.-68G=
NR_134869.1:n.434G=
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