Canonical Allele Identifier: CA412612776

Gene: ARX

Linked Data

• gnomAD v4: X-25013367-C-G
• MyVariant Identifiers: chrX:g.25031484C>G (hg19) ; chrX:g.25013367C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25013367C>G , CM000685.2:g.25013367C>G	GRCh38
NC_000023.10:g.25031484C>G , CM000685.1:g.25031484C>G	GRCh37
NC_000023.9:g.24941405C>G	NCBI36
NG_008281.1:g.7582G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379044.5:c.628G>C MANE Select	ENSP00000368332.4:p.Gly210Arg
ENST00000379044.4:c.628G>C	ENSP00000368332.4:p.Gly210Arg
NM_139058.2:c.628G>C	NP_620689.1:p.Gly210Arg
NM_139058.3:c.628G>C MANE Select	NP_620689.1:p.Gly210Arg