Canonical Allele Identifier: CA412611360

Gene: ARX

Linked Data

• ClinVar Variation Id: 1376496
• ClinVar RCV Id: RCV001885942 ; RCV003154209
• dbSNP Id: rs2147320493
• gnomAD v4: X-25007288-G-A
• MyVariant Identifiers: chrX:g.25025405G>A (hg19) ; chrX:g.25007288G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25007288G>A , CM000685.2:g.25007288G>A	GRCh38
NC_000023.10:g.25025405G>A , CM000685.1:g.25025405G>A	GRCh37
NC_000023.9:g.24935326G>A	NCBI36
NG_008281.1:g.13661C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379044.5:c.1271C>T MANE Select	ENSP00000368332.4:p.Pro424Leu
ENST00000379044.4:c.1271C>T	ENSP00000368332.4:p.Pro424Leu
NM_139058.2:c.1271C>T	NP_620689.1:p.Pro424Leu
NM_139058.3:c.1271C>T MANE Select	NP_620689.1:p.Pro424Leu