Canonical Allele Identifier: CA2420207934
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010009C= , CM000685.2:g.25010009C= GRCh38
NC_000023.10:g.25028126C= , CM000685.1:g.25028126C= GRCh37
NC_000023.9:g.24938047C= NCBI36
NG_008281.1:g.10940G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1119+251G= MANE Select ENSP00000368332.4:n.1119+251G=
ENST00000379044.4:c.1119+251G= ENSP00000368332.4:n.1119+251G=
NM_139058.2:c.1119+251G= NP_620689.1:n.1119+251G=
NM_139058.3:c.1119+251G= MANE Select NP_620689.1:n.1119+251G=