Canonical Allele Identifier: CA2579637382
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010167dup , CM000685.2:g.25010167dup GRCh38
NC_000023.10:g.25028284dup , CM000685.1:g.25028284dup GRCh37
NC_000023.9:g.24938205dup NCBI36
NG_008281.1:g.10782dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1119+93dup MANE Select ENSP00000368332.4:n.1119+93dup
ENST00000379044.4:c.1119+93dup ENSP00000368332.4:n.1119+93dup
NM_139058.2:c.1119+93dup NP_620689.1:n.1119+93dup
NM_139058.3:c.1119+93dup MANE Select NP_620689.1:n.1119+93dup