Canonical Allele Identifier: CA2420209365
Gene: ARX HGNC NCBI

Linked Data

ClinVar Variation Id: 1998762
ClinVar RCV Id: RCV002814889
dbSNP Id: rs2048713060

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013647_25013652dup , CM000685.2:g.25013647_25013652dup GRCh38
NC_000023.10:g.25031764_25031769dup , CM000685.1:g.25031764_25031769dup GRCh37
NC_000023.9:g.24941685_24941690dup NCBI36
NG_008281.1:g.7305_7310dup

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.351_356dup MANE Select ENSP00000368332.4:p.Ala119_Gly120insThrAl...
ENST00000379044.4:c.351_356dup ENSP00000368332.4:p.Ala119_Gly120insThrAl...
NM_139058.2:c.351_356dup NP_620689.1:p.Ala119_Gly120insThrAla
NM_139058.3:c.351_356dup MANE Select NP_620689.1:p.Ala119_Gly120insThrAla