Canonical Allele Identifier: CA412613177
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25013553-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013553C>T , CM000685.2:g.25013553C>T GRCh38
NC_000023.10:g.25031670C>T , CM000685.1:g.25031670C>T GRCh37
NC_000023.9:g.24941591C>T NCBI36
NG_008281.1:g.7396G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.442G>A MANE Select ENSP00000368332.4:p.Ala148Thr
ENST00000379044.4:c.442G>A ENSP00000368332.4:p.Ala148Thr
NM_139058.2:c.442G>A NP_620689.1:p.Ala148Thr
NM_139058.3:c.442G>A MANE Select NP_620689.1:p.Ala148Thr