Canonical Allele Identifier: CA2693353702
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013451del , CM000685.2:g.25013451del GRCh38
NC_000023.10:g.25031568del , CM000685.1:g.25031568del GRCh37
NC_000023.9:g.24941489del NCBI36
NG_008281.1:g.7499del

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.545del MANE Select ENSP00000368332.4:p.Phe182SerfsTer?
ENST00000379044.4:c.545del ENSP00000368332.4:p.Phe182SerfsTer?
NM_139058.2:c.545del NP_620689.1:p.Phe182SerfsTer?
NM_139058.3:c.545del MANE Select NP_620689.1:p.Phe182SerfsTer?