Canonical Allele Identifier: CA2420209434
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013776G= , CM000685.2:g.25013776G= GRCh38
NC_000023.10:g.25031893G= , CM000685.1:g.25031893G= GRCh37
NC_000023.9:g.24941814G= NCBI36
NG_008281.1:g.7173C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.219C= MANE Select ENSP00000368332.4:p.Ala73=
ENST00000379044.4:c.219C= ENSP00000368332.4:p.Ala73=
NM_139058.2:c.219C= NP_620689.1:p.Ala73=
NM_139058.3:c.219C= MANE Select NP_620689.1:p.Ala73=