Canonical Allele Identifier: CA2693353605
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010186_25010187insCCCAA , CM000685.2:g.25010186_25010187insCCCAA GRCh38
NC_000023.10:g.25028303_25028304insCCCAA , CM000685.1:g.25028303_25028304insCCCAA GRCh37
NC_000023.9:g.24938224_24938225insCCCAA NCBI36
NG_008281.1:g.10762_10763insTTGGG

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+73_1119+74insTTGGG MANE Select ENSP00000368332.4:n.1119+73_1119+74insTTG...
ENST00000379044.4:c.1119+73_1119+74insTTGGG ENSP00000368332.4:n.1119+73_1119+74insTTG...
NM_139058.2:c.1119+73_1119+74insTTGGG NP_620689.1:n.1119+73_1119+74insTTGGG
NM_139058.3:c.1119+73_1119+74insTTGGG MANE Select NP_620689.1:n.1119+73_1119+74insTTGGG