Canonical Allele Identifier: CA2420210089
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25015543T= , CM000685.2:g.25015543T= GRCh38
NC_000023.10:g.25033660T= , CM000685.1:g.25033660T= GRCh37
NC_000023.9:g.24943581T= NCBI36
NG_008281.1:g.5406A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.195A= MANE Select ENSP00000368332.4:p.Gln65=
ENST00000379044.4:c.195A= ENSP00000368332.4:p.Gln65=
NM_139058.2:c.195A= NP_620689.1:p.Gln65=
NM_139058.3:c.195A= MANE Select NP_620689.1:p.Gln65=