Canonical Allele Identifier: CA412612613
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013290T>G , CM000685.2:g.25013290T>G GRCh38
NC_000023.10:g.25031407T>G , CM000685.1:g.25031407T>G GRCh37
NC_000023.9:g.24941328T>G NCBI36
NG_008281.1:g.7659A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.705A>C MANE Select ENSP00000368332.4:p.Glu235Asp
ENST00000379044.4:c.705A>C ENSP00000368332.4:p.Glu235Asp
NM_139058.2:c.705A>C NP_620689.1:p.Glu235Asp
NM_139058.3:c.705A>C MANE Select NP_620689.1:p.Glu235Asp