Canonical Allele Identifier: CA412611449
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25007327-C-A
MyVariant Identifiers: chrX:g.25025444C>A (hg19) chrX:g.25007327C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25007327C>A , CM000685.2:g.25007327C>A GRCh38
NC_000023.10:g.25025444C>A , CM000685.1:g.25025444C>A GRCh37
NC_000023.9:g.24935365C>A NCBI36
NG_008281.1:g.13622G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1232G>T MANE Select ENSP00000368332.4:p.Ser411Ile
ENST00000379044.4:c.1232G>T ENSP00000368332.4:p.Ser411Ile
NM_139058.2:c.1232G>T NP_620689.1:p.Ser411Ile
NM_139058.3:c.1232G>T MANE Select NP_620689.1:p.Ser411Ile
Search 100 bp 5'
Search 100 bp 3'