Canonical Allele Identifier: CA412612353
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25013168-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013168G>T , CM000685.2:g.25013168G>T GRCh38
NC_000023.10:g.25031285G>T , CM000685.1:g.25031285G>T GRCh37
NC_000023.9:g.24941206G>T NCBI36
NG_008281.1:g.7781C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.827C>A MANE Select ENSP00000368332.4:p.Ala276Glu
ENST00000379044.4:c.827C>A ENSP00000368332.4:p.Ala276Glu
NM_139058.2:c.827C>A NP_620689.1:p.Ala276Glu
NM_139058.3:c.827C>A MANE Select NP_620689.1:p.Ala276Glu