Canonical Allele Identifier: CA2693353413
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013161_25013190del , CM000685.2:g.25013161_25013190del GRCh38
NC_000023.10:g.25031278_25031307del , CM000685.1:g.25031278_25031307del GRCh37
NC_000023.9:g.24941199_24941228del NCBI36
NG_008281.1:g.7764_7793del

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.810_839del MANE Select ENSP00000368332.4:p.Thr271_Ala280del
ENST00000379044.4:c.810_839del ENSP00000368332.4:p.Thr271_Ala280del
NM_139058.2:c.810_839del NP_620689.1:p.Thr271_Ala280del
NM_139058.3:c.810_839del MANE Select NP_620689.1:p.Thr271_Ala280del