Canonical Allele Identifier: CA412613169
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25013550-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013550C>A , CM000685.2:g.25013550C>A GRCh38
NC_000023.10:g.25031667C>A , CM000685.1:g.25031667C>A GRCh37
NC_000023.9:g.24941588C>A NCBI36
NG_008281.1:g.7399G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.445G>T MANE Select ENSP00000368332.4:p.Ala149Ser
ENST00000379044.4:c.445G>T ENSP00000368332.4:p.Ala149Ser
NM_139058.2:c.445G>T NP_620689.1:p.Ala149Ser
NM_139058.3:c.445G>T MANE Select NP_620689.1:p.Ala149Ser