Canonical Allele Identifier: CA412612598
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013285T>A , CM000685.2:g.25013285T>A GRCh38
NC_000023.10:g.25031402T>A , CM000685.1:g.25031402T>A GRCh37
NC_000023.9:g.24941323T>A NCBI36
NG_008281.1:g.7664A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.710A>T MANE Select ENSP00000368332.4:p.Glu237Val
ENST00000379044.4:c.710A>T ENSP00000368332.4:p.Glu237Val
NM_139058.2:c.710A>T NP_620689.1:p.Glu237Val
NM_139058.3:c.710A>T MANE Select NP_620689.1:p.Glu237Val