Canonical Allele Identifier: CA412613433
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013682C>A , CM000685.2:g.25013682C>A GRCh38
NC_000023.10:g.25031799C>A , CM000685.1:g.25031799C>A GRCh37
NC_000023.9:g.24941720C>A NCBI36
NG_008281.1:g.7267G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.313G>T MANE Select ENSP00000368332.4:p.Ala105Ser
ENST00000379044.4:c.313G>T ENSP00000368332.4:p.Ala105Ser
NM_139058.2:c.313G>T NP_620689.1:p.Ala105Ser
NM_139058.3:c.313G>T MANE Select NP_620689.1:p.Ala105Ser