Canonical Allele Identifier: CA2420209299
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013528_25013543delinsCAGGCCGCGGCGGCCG , CM000685.2:g.25013528_25013543delinsCAGGCCGCGGCGGCCG GRCh38
NC_000023.10:g.25031645_25031660delinsCAGGCCGCGGCGGCCG , CM000685.1:g.25031645_25031660delinsCAGGCCGCGGCGGCCG GRCh37
NC_000023.9:g.24941566_24941581delinsCAGGCCGCGGCGGCCG NCBI36
NG_008281.1:g.7406_7421delinsCGGCCGCCGCGGCCTG

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.452_467delinsCGGCCGCCGCGGCCTG MANE Select ENSP00000368332.4:p.Ala151=
ENST00000379044.4:c.452_467delinsCGGCCGCCGCGGCCTG ENSP00000368332.4:p.Ala151=
NM_139058.2:c.452_467delinsCGGCCGCCGCGGCCTG NP_620689.1:p.Ala151=
NM_139058.3:c.452_467delinsCGGCCGCCGCGGCCTG MANE Select NP_620689.1:p.Ala151=