Canonical Allele Identifier: CA2420208032
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010262G= , CM000685.2:g.25010262G= GRCh38
NC_000023.10:g.25028379G= , CM000685.1:g.25028379G= GRCh37
NC_000023.9:g.24938300G= NCBI36
NG_008281.1:g.10687C=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1117C= MANE Select ENSP00000368332.4:p.Gln373=
ENST00000379044.4:c.1117C= ENSP00000368332.4:p.Gln373=
NM_139058.2:c.1117C= NP_620689.1:p.Gln373=
NM_139058.3:c.1117C= MANE Select NP_620689.1:p.Gln373=