Canonical Allele Identifier: CA2420209324
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 2201778
ClinVar RCV Id: RCV002644499
dbSNP Id: rs2048712443

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013553_25013554insGGCCGC , CM000685.2:g.25013553_25013554insGGCCGC GRCh38
NC_000023.10:g.25031670_25031671insGGCCGC , CM000685.1:g.25031670_25031671insGGCCGC GRCh37
NC_000023.9:g.24941591_24941592insGGCCGC NCBI36
NG_008281.1:g.7397_7398insGGCCGC

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.443_444insGGCCGC MANE Select ENSP00000368332.4:p.Ala148_Ala149insAlaAl...
ENST00000379044.4:c.443_444insGGCCGC ENSP00000368332.4:p.Ala148_Ala149insAlaAl...
NM_139058.2:c.443_444insGGCCGC NP_620689.1:p.Ala148_Ala149insAlaAla
NM_139058.3:c.443_444insGGCCGC MANE Select NP_620689.1:p.Ala148_Ala149insAlaAla