Canonical Allele Identifier: CA2420208998
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012828_25012829delinsGC , CM000685.2:g.25012828_25012829delinsGC GRCh38
NC_000023.10:g.25030945_25030946delinsGC , CM000685.1:g.25030945_25030946delinsGC GRCh37
NC_000023.9:g.24940866_24940867delinsGC NCBI36
NG_008281.1:g.8120_8121delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1073+93_1073+94delinsGC MANE Select ENSP00000368332.4:n.1073+93_1073+94delinsGC
ENST00000379044.4:c.1073+93_1073+94delinsGC ENSP00000368332.4:n.1073+93_1073+94delinsGC
NM_139058.2:c.1073+93_1073+94delinsGC NP_620689.1:n.1073+93_1073+94delinsGC
NM_139058.3:c.1073+93_1073+94delinsGC MANE Select NP_620689.1:n.1073+93_1073+94delinsGC