Canonical Allele Identifier: CA2420205969
Gene: ARX HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004863G= , CM000685.2:g.25004863G= GRCh38
NC_000023.10:g.25022980G= , CM000685.1:g.25022980G= GRCh37
NC_000023.9:g.24932901G= NCBI36
NG_008281.1:g.16086C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1496C= MANE Select ENSP00000368332.4:p.Ala499=
ENST00000636885.1:n.84C=
ENST00000379044.4:c.1496C= ENSP00000368332.4:p.Ala499=
NM_139058.2:c.1496C= NP_620689.1:p.Ala499=
NM_139058.3:c.1496C= MANE Select NP_620689.1:p.Ala499=
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