Canonical Allele Identifier: CA412612147
Gene: ARX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.25031186T>A (hg19) chrX:g.25013069T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013069T>A , CM000685.2:g.25013069T>A GRCh38
NC_000023.10:g.25031186T>A , CM000685.1:g.25031186T>A GRCh37
NC_000023.9:g.24941107T>A NCBI36
NG_008281.1:g.7880A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.926A>T MANE Select ENSP00000368332.4:p.Asp309Val
ENST00000379044.4:c.926A>T ENSP00000368332.4:p.Asp309Val
NM_139058.2:c.926A>T NP_620689.1:p.Asp309Val
NM_139058.3:c.926A>T MANE Select NP_620689.1:p.Asp309Val
Search 100 bp 5'
Search 100 bp 3'