Canonical Allele Identifier: CA1131756224
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010172_25010173dup , CM000685.2:g.25010172_25010173dup GRCh38
NC_000023.10:g.25028289_25028290dup , CM000685.1:g.25028289_25028290dup GRCh37
NC_000023.9:g.24938210_24938211dup NCBI36
NG_008281.1:g.10780_10781dup

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+91_1119+92dup MANE Select ENSP00000368332.4:n.1119+91_1119+92dup
ENST00000379044.4:c.1119+91_1119+92dup ENSP00000368332.4:n.1119+91_1119+92dup
NM_139058.2:c.1119+91_1119+92dup NP_620689.1:n.1119+91_1119+92dup
NM_139058.3:c.1119+91_1119+92dup MANE Select NP_620689.1:n.1119+91_1119+92dup