Canonical Allele Identifier: CA2740092063
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 2943777
ClinVar RCV Id: RCV003803335

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004802del , CM000685.2:g.25004802del GRCh38
NC_000023.10:g.25022919del , CM000685.1:g.25022919del GRCh37
NC_000023.9:g.24932840del NCBI36
NG_008281.1:g.16149del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1559del MANE Select ENSP00000368332.4:p.Pro520ArgfsTer13
ENST00000379044.4:c.1559del ENSP00000368332.4:p.Pro520ArgfsTer13
NM_139058.2:c.1559del NP_620689.1:p.Pro520ArgfsTer13
NM_139058.3:c.1559del MANE Select NP_620689.1:p.Pro520ArgfsTer13