Canonical Allele Identifier: CA2693353732
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013627_25013674del , CM000685.2:g.25013627_25013674del GRCh38
NC_000023.10:g.25031744_25031791del , CM000685.1:g.25031744_25031791del GRCh37
NC_000023.9:g.24941665_24941712del NCBI36
NG_008281.1:g.7277_7324del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.323_370del MANE Select ENSP00000368332.4:p.Ala108_Gly123del
ENST00000379044.4:c.323_370del ENSP00000368332.4:p.Ala108_Gly123del
NM_139058.2:c.323_370del NP_620689.1:p.Ala108_Gly123del
NM_139058.3:c.323_370del MANE Select NP_620689.1:p.Ala108_Gly123del