Canonical Allele Identifier: CA412613442
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25013687-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013687G>A , CM000685.2:g.25013687G>A GRCh38
NC_000023.10:g.25031804G>A , CM000685.1:g.25031804G>A GRCh37
NC_000023.9:g.24941725G>A NCBI36
NG_008281.1:g.7262C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.308C>T MANE Select ENSP00000368332.4:p.Ala103Val
ENST00000379044.4:c.308C>T ENSP00000368332.4:p.Ala103Val
NM_139058.2:c.308C>T NP_620689.1:p.Ala103Val
NM_139058.3:c.308C>T MANE Select NP_620689.1:p.Ala103Val