Canonical Allele Identifier: CA412610564
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25004708-T-G
MyVariant Identifiers: chrX:g.25022825T>G (hg19) chrX:g.25004708T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004708T>G , CM000685.2:g.25004708T>G GRCh38
NC_000023.10:g.25022825T>G , CM000685.1:g.25022825T>G GRCh37
NC_000023.9:g.24932746T>G NCBI36
NG_008281.1:g.16241A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1651A>C MANE Select ENSP00000368332.4:p.Ile551Leu
ENST00000379044.4:c.1651A>C ENSP00000368332.4:p.Ile551Leu
NM_139058.2:c.1651A>C NP_620689.1:p.Ile551Leu
NM_139058.3:c.1651A>C MANE Select NP_620689.1:p.Ile551Leu
Search 100 bp 5'
Search 100 bp 3'