Canonical Allele Identifier: CA2420209302
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013529_25013538delinsAGGCCGCGGC , CM000685.2:g.25013529_25013538delinsAGGCCGCGGC GRCh38
NC_000023.10:g.25031646_25031655delinsAGGCCGCGGC , CM000685.1:g.25031646_25031655delinsAGGCCGCGGC GRCh37
NC_000023.9:g.24941567_24941576delinsAGGCCGCGGC NCBI36
NG_008281.1:g.7411_7420delinsGCCGCGGCCT

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.457_466delinsGCCGCGGCCT MANE Select ENSP00000368332.4:p.Ala153=
ENST00000379044.4:c.457_466delinsGCCGCGGCCT ENSP00000368332.4:p.Ala153=
NM_139058.2:c.457_466delinsGCCGCGGCCT NP_620689.1:p.Ala153=
NM_139058.3:c.457_466delinsGCCGCGGCCT MANE Select NP_620689.1:p.Ala153=