Canonical Allele Identifier: CA2420207028
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25007187C= , CM000685.2:g.25007187C= GRCh38
NC_000023.10:g.25025304C= , CM000685.1:g.25025304C= GRCh37
NC_000023.9:g.24935225C= NCBI36
NG_008281.1:g.13762G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1372G= MANE Select ENSP00000368332.4:p.Ala458=
ENST00000379044.4:c.1372G= ENSP00000368332.4:p.Ala458=
NM_139058.2:c.1372G= NP_620689.1:p.Ala458=
NM_139058.3:c.1372G= MANE Select NP_620689.1:p.Ala458=