Canonical Allele Identifier: CA2420207951
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010076_25010077delinsAT , CM000685.2:g.25010076_25010077delinsAT GRCh38
NC_000023.10:g.25028193_25028194delinsAT , CM000685.1:g.25028193_25028194delinsAT GRCh37
NC_000023.9:g.24938114_24938115delinsAT NCBI36
NG_008281.1:g.10872_10873delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+183_1119+184delinsAT MANE Select ENSP00000368332.4:n.1119+183_1119+184deli...
ENST00000379044.4:c.1119+183_1119+184delinsAT ENSP00000368332.4:n.1119+183_1119+184deli...
NM_139058.2:c.1119+183_1119+184delinsAT NP_620689.1:n.1119+183_1119+184delinsAT
NM_139058.3:c.1119+183_1119+184delinsAT MANE Select NP_620689.1:n.1119+183_1119+184delinsAT