Canonical Allele Identifier: CA171147
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 157749
ClinVar RCV Id: RCV000145048
dbSNP Id: rs587783192

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004817del , CM000685.2:g.25004817del GRCh38
NC_000023.10:g.25022934del , CM000685.1:g.25022934del GRCh37
NC_000023.9:g.24932855del NCBI36
NG_008281.1:g.16134del

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1544del MANE Select ENSP00000368332.4:p.Gly515AlafsTer18
ENST00000379044.4:c.1544del ENSP00000368332.4:p.Gly515AlafsTer18
NM_139058.2:c.1544del NP_620689.1:p.Gly515AlafsTer18
NM_139058.3:c.1544del MANE Select NP_620689.1:p.Gly515AlafsTer18