Canonical Allele Identifier: CA2693353645
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010195_25010196insAAA , CM000685.2:g.25010195_25010196insAAA GRCh38
NC_000023.10:g.25028312_25028313insAAA , CM000685.1:g.25028312_25028313insAAA GRCh37
NC_000023.9:g.24938233_24938234insAAA NCBI36
NG_008281.1:g.10754_10755insTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+65_1119+66insTTT MANE Select ENSP00000368332.4:n.1119+65_1119+66insTTT...
ENST00000379044.4:c.1119+65_1119+66insTTT ENSP00000368332.4:n.1119+65_1119+66insTTT...
NM_139058.2:c.1119+65_1119+66insTTT NP_620689.1:n.1119+65_1119+66insTTT
NM_139058.3:c.1119+65_1119+66insTTT MANE Select NP_620689.1:n.1119+65_1119+66insTTT