Canonical Allele Identifier: CA2420208009
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010205C= , CM000685.2:g.25010205C= GRCh38
NC_000023.10:g.25028322C= , CM000685.1:g.25028322C= GRCh37
NC_000023.9:g.24938243C= NCBI36
NG_008281.1:g.10744G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+55G= MANE Select ENSP00000368332.4:n.1119+55G=
ENST00000379044.4:c.1119+55G= ENSP00000368332.4:n.1119+55G=
NM_139058.2:c.1119+55G= NP_620689.1:n.1119+55G=
NM_139058.3:c.1119+55G= MANE Select NP_620689.1:n.1119+55G=