Canonical Allele Identifier: CA412612558
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013270T>A , CM000685.2:g.25013270T>A GRCh38
NC_000023.10:g.25031387T>A , CM000685.1:g.25031387T>A GRCh37
NC_000023.9:g.24941308T>A NCBI36
NG_008281.1:g.7679A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.725A>T MANE Select ENSP00000368332.4:p.Glu242Val
ENST00000379044.4:c.725A>T ENSP00000368332.4:p.Glu242Val
NM_139058.2:c.725A>T NP_620689.1:p.Glu242Val
NM_139058.3:c.725A>T MANE Select NP_620689.1:p.Glu242Val