Canonical Allele Identifier: CA412611775

Gene: ARX

Linked Data

• gnomAD v4: X-25010292-T-G
• MyVariant Identifiers: chrX:g.25028409T>G (hg19) ; chrX:g.25010292T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.25010292T>G , CM000685.2:g.25010292T>G	GRCh38
NC_000023.10:g.25028409T>G , CM000685.1:g.25028409T>G	GRCh37
NC_000023.9:g.24938330T>G	NCBI36
NG_008281.1:g.10657A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379044.5:c.1087A>C MANE Select	ENSP00000368332.4:p.Met363Leu
ENST00000379044.4:c.1087A>C	ENSP00000368332.4:p.Met363Leu
NM_139058.2:c.1087A>C	NP_620689.1:p.Met363Leu
NM_139058.3:c.1087A>C MANE Select	NP_620689.1:p.Met363Leu