Canonical Allele Identifier: CA2580618167
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 2581045
ClinVar RCV Id: RCV003330280

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013174dup , CM000685.2:g.25013174dup GRCh38
NC_000023.10:g.25031291dup , CM000685.1:g.25031291dup GRCh37
NC_000023.9:g.24941212dup NCBI36
NG_008281.1:g.7775dup

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.821dup MANE Select ENSP00000368332.4:p.Ala275GlyfsTer29
ENST00000379044.4:c.821dup ENSP00000368332.4:p.Ala275GlyfsTer29
NM_139058.2:c.821dup NP_620689.1:p.Ala275GlyfsTer29
NM_139058.3:c.821dup MANE Select NP_620689.1:p.Ala275GlyfsTer29