Canonical Allele Identifier: CA412610968
Gene: ARX HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.25023021A>C (hg19) chrX:g.25004904A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004904A>C , CM000685.2:g.25004904A>C GRCh38
NC_000023.10:g.25023021A>C , CM000685.1:g.25023021A>C GRCh37
NC_000023.9:g.24932942A>C NCBI36
NG_008281.1:g.16045T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1455T>G MANE Select ENSP00000368332.4:p.Phe485Leu
ENST00000636885.1:n.43T>G
ENST00000379044.4:c.1455T>G ENSP00000368332.4:p.Phe485Leu
NM_139058.2:c.1455T>G NP_620689.1:p.Phe485Leu
NM_139058.3:c.1455T>G MANE Select NP_620689.1:p.Phe485Leu
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