Canonical Allele Identifier: CA412610901
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25004870-C-A
MyVariant Identifiers: chrX:g.25022987C>A (hg19) chrX:g.25004870C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004870C>A , CM000685.2:g.25004870C>A GRCh38
NC_000023.10:g.25022987C>A , CM000685.1:g.25022987C>A GRCh37
NC_000023.9:g.24932908C>A NCBI36
NG_008281.1:g.16079G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1489G>T MANE Select ENSP00000368332.4:p.Ala497Ser
ENST00000636885.1:n.77G>T
ENST00000379044.4:c.1489G>T ENSP00000368332.4:p.Ala497Ser
NM_139058.2:c.1489G>T NP_620689.1:p.Ala497Ser
NM_139058.3:c.1489G>T MANE Select NP_620689.1:p.Ala497Ser
Search 100 bp 5'
Search 100 bp 3'