Canonical Allele Identifier: CA2420207957
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010105_25010107delinsTGA , CM000685.2:g.25010105_25010107delinsTGA GRCh38
NC_000023.10:g.25028222_25028224delinsTGA , CM000685.1:g.25028222_25028224delinsTGA GRCh37
NC_000023.9:g.24938143_24938145delinsTGA NCBI36
NG_008281.1:g.10842_10844delinsTCA

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+153_1119+155delinsTCA MANE Select ENSP00000368332.4:n.1119+153_1119+155deli...
ENST00000379044.4:c.1119+153_1119+155delinsTCA ENSP00000368332.4:n.1119+153_1119+155deli...
NM_139058.2:c.1119+153_1119+155delinsTCA NP_620689.1:n.1119+153_1119+155delinsTCA
NM_139058.3:c.1119+153_1119+155delinsTCA MANE Select NP_620689.1:n.1119+153_1119+155delinsTCA