Canonical Allele Identifier: CA2420206882
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25006825T= , CM000685.2:g.25006825T= GRCh38
NC_000023.10:g.25024942T= , CM000685.1:g.25024942T= GRCh37
NC_000023.9:g.24934863T= NCBI36
NG_008281.1:g.14124A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1448+286A= MANE Select ENSP00000368332.4:n.1448+286A=
ENST00000637993.1:c.62-198A=
ENST00000379044.4:c.1448+286A= ENSP00000368332.4:n.1448+286A=
NM_139058.2:c.1448+286A= NP_620689.1:n.1448+286A=
NM_139058.3:c.1448+286A= MANE Select NP_620689.1:n.1448+286A=