Canonical Allele Identifier: CA2693353627
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010194_25010195insCAC , CM000685.2:g.25010194_25010195insCAC GRCh38
NC_000023.10:g.25028311_25028312insCAC , CM000685.1:g.25028311_25028312insCAC GRCh37
NC_000023.9:g.24938232_24938233insCAC NCBI36
NG_008281.1:g.10755_10756insTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+66_1119+67insTGG MANE Select ENSP00000368332.4:n.1119+66_1119+67insTGG...
ENST00000379044.4:c.1119+66_1119+67insTGG ENSP00000368332.4:n.1119+66_1119+67insTGG...
NM_139058.2:c.1119+66_1119+67insTGG NP_620689.1:n.1119+66_1119+67insTGG
NM_139058.3:c.1119+66_1119+67insTGG MANE Select NP_620689.1:n.1119+66_1119+67insTGG