Canonical Allele Identifier: CA515947031
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 2944887
ClinVar RCV Id: RCV003808589
gnomAD v4: X-25007239-G-A
MyVariant Identifiers: chrX:g.25025356G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25007239G>A , CM000685.2:g.25007239G>A GRCh38
NC_000023.10:g.25025356G>A , CM000685.1:g.25025356G>A GRCh37
NC_000023.9:g.24935277G>A NCBI36
NG_008281.1:g.13710C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1320C>T MANE Select ENSP00000368332.4:p.Ala440=
ENST00000379044.4:c.1320C>T ENSP00000368332.4:p.Ala440=
NM_139058.2:c.1320C>T NP_620689.1:p.Ala440=
NM_139058.3:c.1320C>T MANE Select NP_620689.1:p.Ala440=