Canonical Allele Identifier: CA412611050

Gene: ARX

Linked Data

• MyVariant Identifiers: chrX:g.25025253C>T (hg19) ; chrX:g.25007136C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25007136C>T , CM000685.2:g.25007136C>T	GRCh38
NC_000023.10:g.25025253C>T , CM000685.1:g.25025253C>T	GRCh37
NC_000023.9:g.24935174C>T	NCBI36
NG_008281.1:g.13813G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379044.5:c.1423G>A MANE Select	ENSP00000368332.4:p.Ala475Thr
ENST00000637993.1:c.36G>A
ENST00000379044.4:c.1423G>A	ENSP00000368332.4:p.Ala475Thr
NM_139058.2:c.1423G>A	NP_620689.1:p.Ala475Thr
NM_139058.3:c.1423G>A MANE Select	NP_620689.1:p.Ala475Thr