Canonical Allele Identifier: CA412611787
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010299T>A , CM000685.2:g.25010299T>A GRCh38
NC_000023.10:g.25028416T>A , CM000685.1:g.25028416T>A GRCh37
NC_000023.9:g.24938337T>A NCBI36
NG_008281.1:g.10650A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1080A>T MANE Select ENSP00000368332.4:p.Glu360Asp
ENST00000379044.4:c.1080A>T ENSP00000368332.4:p.Glu360Asp
NM_139058.2:c.1080A>T NP_620689.1:p.Glu360Asp
NM_139058.3:c.1080A>T MANE Select NP_620689.1:p.Glu360Asp