Canonical Allele Identifier: CA2420209364
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013638C= , CM000685.2:g.25013638C= GRCh38
NC_000023.10:g.25031755C= , CM000685.1:g.25031755C= GRCh37
NC_000023.9:g.24941676C= NCBI36
NG_008281.1:g.7311G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.357G= MANE Select ENSP00000368332.4:p.Ala119=
ENST00000379044.4:c.357G= ENSP00000368332.4:p.Ala119=
NM_139058.2:c.357G= NP_620689.1:p.Ala119=
NM_139058.3:c.357G= MANE Select NP_620689.1:p.Ala119=