Canonical Allele Identifier: CA2420205879
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004654G= , CM000685.2:g.25004654G= GRCh38
NC_000023.10:g.25022771G= , CM000685.1:g.25022771G= GRCh37
NC_000023.9:g.24932692G= NCBI36
NG_008281.1:g.16295C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.*16C= MANE Select ENSP00000368332.4:n.*16C=
ENST00000379044.4:c.*16C= ENSP00000368332.4:n.*16C=
NM_139058.2:c.*16C= NP_620689.1:n.*16C=
NM_139058.3:c.*16C= MANE Select NP_620689.1:n.*16C=