Canonical Allele Identifier: CA2693353531
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010129del , CM000685.2:g.25010129del GRCh38
NC_000023.10:g.25028246del , CM000685.1:g.25028246del GRCh37
NC_000023.9:g.24938167del NCBI36
NG_008281.1:g.10823del

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+134del MANE Select ENSP00000368332.4:n.1119+134del
ENST00000379044.4:c.1119+134del ENSP00000368332.4:n.1119+134del
NM_139058.2:c.1119+134del NP_620689.1:n.1119+134del
NM_139058.3:c.1119+134del MANE Select NP_620689.1:n.1119+134del