Canonical Allele Identifier: CA412611047

Gene: ARX

Linked Data

• MyVariant Identifiers: chrX:g.25025252G>C (hg19) ; chrX:g.25007135G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25007135G>C , CM000685.2:g.25007135G>C	GRCh38
NC_000023.10:g.25025252G>C , CM000685.1:g.25025252G>C	GRCh37
NC_000023.9:g.24935173G>C	NCBI36
NG_008281.1:g.13814C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379044.5:c.1424C>G MANE Select	ENSP00000368332.4:p.Ala475Gly
ENST00000637993.1:c.37C>G
ENST00000379044.4:c.1424C>G	ENSP00000368332.4:p.Ala475Gly
NM_139058.2:c.1424C>G	NP_620689.1:p.Ala475Gly
NM_139058.3:c.1424C>G MANE Select	NP_620689.1:p.Ala475Gly