Canonical Allele Identifier: CA2580100526
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 2059968
ClinVar RCV Id: RCV002938665

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010270del , CM000685.2:g.25010270del GRCh38
NC_000023.10:g.25028387del , CM000685.1:g.25028387del GRCh37
NC_000023.9:g.24938308del NCBI36
NG_008281.1:g.10681del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1111del MANE Select ENSP00000368332.4:p.Arg371GlufsTer?
ENST00000379044.4:c.1111del ENSP00000368332.4:p.Arg371GlufsTer?
NM_139058.2:c.1111del NP_620689.1:p.Arg371GlufsTer?
NM_139058.3:c.1111del MANE Select NP_620689.1:p.Arg371GlufsTer?