Canonical Allele Identifier: CA412612078
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013039G>C , CM000685.2:g.25013039G>C GRCh38
NC_000023.10:g.25031156G>C , CM000685.1:g.25031156G>C GRCh37
NC_000023.9:g.24941077G>C NCBI36
NG_008281.1:g.7910C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.956C>G MANE Select ENSP00000368332.4:p.Ser319Trp
ENST00000379044.4:c.956C>G ENSP00000368332.4:p.Ser319Trp
NM_139058.2:c.956C>G NP_620689.1:p.Ser319Trp
NM_139058.3:c.956C>G MANE Select NP_620689.1:p.Ser319Trp