Canonical Allele Identifier: CA515947468
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25007419-C-T
MyVariant Identifiers: chrX:g.25025536C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25007419C>T , CM000685.2:g.25007419C>T GRCh38
NC_000023.10:g.25025536C>T , CM000685.1:g.25025536C>T GRCh37
NC_000023.9:g.24935457C>T NCBI36
NG_008281.1:g.13530G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1140G>A MANE Select ENSP00000368332.4:p.Arg380=
ENST00000379044.4:c.1140G>A ENSP00000368332.4:p.Arg380=
NM_139058.2:c.1140G>A NP_620689.1:p.Arg380=
NM_139058.3:c.1140G>A MANE Select NP_620689.1:p.Arg380=