Canonical Allele Identifier: CA412612967

Gene: ARX

Linked Data

• MyVariant Identifiers: chrX:g.25031579T>G (hg19) ; chrX:g.25013462T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25013462T>G , CM000685.2:g.25013462T>G	GRCh38
NC_000023.10:g.25031579T>G , CM000685.1:g.25031579T>G	GRCh37
NC_000023.9:g.24941500T>G	NCBI36
NG_008281.1:g.7487A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379044.5:c.533A>C MANE Select	ENSP00000368332.4:p.Asn178Thr
ENST00000379044.4:c.533A>C	ENSP00000368332.4:p.Asn178Thr
NM_139058.2:c.533A>C	NP_620689.1:p.Asn178Thr
NM_139058.3:c.533A>C MANE Select	NP_620689.1:p.Asn178Thr