Canonical Allele Identifier: CA2530386685
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013170_25013171del , CM000685.2:g.25013170_25013171del GRCh38
NC_000023.10:g.25031287_25031288del , CM000685.1:g.25031287_25031288del GRCh37
NC_000023.9:g.24941208_24941209del NCBI36
NG_008281.1:g.7778_7779del

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.824_825del MANE Select ENSP00000368332.4:p.Ala275GlyfsTer28
ENST00000379044.4:c.824_825del ENSP00000368332.4:p.Ala275GlyfsTer28
NM_139058.2:c.824_825del NP_620689.1:p.Ala275GlyfsTer28
NM_139058.3:c.824_825del MANE Select NP_620689.1:p.Ala275GlyfsTer28