Canonical Allele Identifier: CA2186761737
Gene: HEXA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.72376044A= , CM000677.2:g.72376044A= GRCh38
NC_000015.9:g.72668385A= , CM000677.1:g.72668385A= GRCh37
NC_000015.8:g.70455439A= NCBI36
NG_009017.1:g.5136T=
NG_009017.2:g.5136T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268097.9:c.-72T= ENSP00000268097.5:n.-72T=
ENST00000569509.5:n.147-213T=
NM_000520.4:c.-72T= NP_000511.2:n.-72T=
NM_000520.5:c.-72T= NP_000511.2:n.-72T=
NM_001318825.1:c.-72T= NP_001305754.1:n.-72T=
NR_134869.1:n.430T=