Canonical Allele Identifier: CA515947403
Gene: ARX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.25025509T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25007392T>A , CM000685.2:g.25007392T>A GRCh38
NC_000023.10:g.25025509T>A , CM000685.1:g.25025509T>A GRCh37
NC_000023.9:g.24935430T>A NCBI36
NG_008281.1:g.13557A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1167A>T MANE Select ENSP00000368332.4:p.Ala389=
ENST00000379044.4:c.1167A>T ENSP00000368332.4:p.Ala389=
NM_139058.2:c.1167A>T NP_620689.1:p.Ala389=
NM_139058.3:c.1167A>T MANE Select NP_620689.1:p.Ala389=
Search 100 bp 5'
Search 100 bp 3'