Canonical Allele Identifier: CA2695232859
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012991_25012999del , CM000685.2:g.25012991_25012999del GRCh38
NC_000023.10:g.25031108_25031116del , CM000685.1:g.25031108_25031116del GRCh37
NC_000023.9:g.24941029_24941037del NCBI36
NG_008281.1:g.7955_7963del

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1001_1009del MANE Select ENSP00000368332.4:p.Thr334_Thr336del
ENST00000379044.4:c.1001_1009del ENSP00000368332.4:p.Thr334_Thr336del
NM_139058.2:c.1001_1009del NP_620689.1:p.Thr334_Thr336del
NM_139058.3:c.1001_1009del MANE Select NP_620689.1:p.Thr334_Thr336del