Canonical Allele Identifier: CA2693353546
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25010161-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010161G>T , CM000685.2:g.25010161G>T GRCh38
NC_000023.10:g.25028278G>T , CM000685.1:g.25028278G>T GRCh37
NC_000023.9:g.24938199G>T NCBI36
NG_008281.1:g.10788C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+99C>A MANE Select ENSP00000368332.4:n.1119+99C>A
ENST00000379044.4:c.1119+99C>A ENSP00000368332.4:n.1119+99C>A
NM_139058.2:c.1119+99C>A NP_620689.1:n.1119+99C>A
NM_139058.3:c.1119+99C>A MANE Select NP_620689.1:n.1119+99C>A