Canonical Allele Identifier: CA2420206883
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25006827C= , CM000685.2:g.25006827C= GRCh38
NC_000023.10:g.25024944C= , CM000685.1:g.25024944C= GRCh37
NC_000023.9:g.24934865C= NCBI36
NG_008281.1:g.14122G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1448+284G= MANE Select ENSP00000368332.4:n.1448+284G=
ENST00000637993.1:c.62-200G=
ENST00000379044.4:c.1448+284G= ENSP00000368332.4:n.1448+284G=
NM_139058.2:c.1448+284G= NP_620689.1:n.1448+284G=
NM_139058.3:c.1448+284G= MANE Select NP_620689.1:n.1448+284G=