Canonical Allele Identifier: CA2420205830
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004571C= , CM000685.2:g.25004571C= GRCh38
NC_000023.10:g.25022688C= , CM000685.1:g.25022688C= GRCh37
NC_000023.9:g.24932609C= NCBI36
NG_008281.1:g.16378G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.*99G= MANE Select ENSP00000368332.4:n.*99G=
ENST00000379044.4:c.*99G= ENSP00000368332.4:n.*99G=
NM_139058.2:c.*99G= NP_620689.1:n.*99G=
NM_139058.3:c.*99G= MANE Select NP_620689.1:n.*99G=