Canonical Allele Identifier: CA2693353440
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013176_25013193dup , CM000685.2:g.25013176_25013193dup GRCh38
NC_000023.10:g.25031293_25031310dup , CM000685.1:g.25031293_25031310dup GRCh37
NC_000023.9:g.24941214_24941231dup NCBI36
NG_008281.1:g.7764_7781dup

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.810_827dup MANE Select ENSP00000368332.4:p.Ala276_Ala277insThrGl...
ENST00000379044.4:c.810_827dup ENSP00000368332.4:p.Ala276_Ala277insThrGl...
NM_139058.2:c.810_827dup NP_620689.1:p.Ala276_Ala277insThrGlyAlaVa...
NM_139058.3:c.810_827dup MANE Select NP_620689.1:p.Ala276_Ala277insThrGlyAlaVa...