Canonical Allele Identifier: CA2693353583
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010176dup , CM000685.2:g.25010176dup GRCh38
NC_000023.10:g.25028293dup , CM000685.1:g.25028293dup GRCh37
NC_000023.9:g.24938214dup NCBI36
NG_008281.1:g.10773dup

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+84dup MANE Select ENSP00000368332.4:n.1119+84dup
ENST00000379044.4:c.1119+84dup ENSP00000368332.4:n.1119+84dup
NM_139058.2:c.1119+84dup NP_620689.1:n.1119+84dup
NM_139058.3:c.1119+84dup MANE Select NP_620689.1:n.1119+84dup