Canonical Allele Identifier: CA2420207939
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010041C= , CM000685.2:g.25010041C= GRCh38
NC_000023.10:g.25028158C= , CM000685.1:g.25028158C= GRCh37
NC_000023.9:g.24938079C= NCBI36
NG_008281.1:g.10908G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1119+219G= MANE Select ENSP00000368332.4:n.1119+219G=
ENST00000379044.4:c.1119+219G= ENSP00000368332.4:n.1119+219G=
NM_139058.2:c.1119+219G= NP_620689.1:n.1119+219G=
NM_139058.3:c.1119+219G= MANE Select NP_620689.1:n.1119+219G=