Canonical Allele Identifier: CA2499226598
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 1070790
dbSNP Id: rs2147324381

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013677_25013697dup , CM000685.2:g.25013677_25013697dup GRCh38
NC_000023.10:g.25031794_25031814dup , CM000685.1:g.25031794_25031814dup GRCh37
NC_000023.9:g.24941715_24941735dup NCBI36
NG_008281.1:g.7257_7277dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.303_323dup MANE Select ENSP00000368332.4:p.Ala108_Ala109insAlaAlaAlaAlaAlaAlaAla
ENST00000379044.4:c.303_323dup ENSP00000368332.4:p.Ala108_Ala109insAlaAlaAlaAlaAlaAlaAla
NM_139058.2:c.303_323dup NP_620689.1:p.Ala108_Ala109insAlaAlaAlaAlaAlaAlaAla
NM_139058.3:c.303_323dup MANE Select NP_620689.1:p.Ala108_Ala109insAlaAlaAlaAlaAlaAlaAla