Canonical Allele Identifier: CA2186761739
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72376047T= , CM000677.2:g.72376047T= GRCh38
NC_000015.9:g.72668388T= , CM000677.1:g.72668388T= GRCh37
NC_000015.8:g.70455442T= NCBI36
NG_009017.1:g.5133A=
NG_009017.2:g.5133A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268097.9:c.-75A= ENSP00000268097.5:n.-75A=
ENST00000569509.5:n.147-216A=
NM_000520.4:c.-75A= NP_000511.2:n.-75A=
NM_000520.5:c.-75A= NP_000511.2:n.-75A=
NM_001318825.1:c.-75A= NP_001305754.1:n.-75A=
NR_134869.1:n.427A=