Canonical Allele Identifier: CA412610938
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004890G>C , CM000685.2:g.25004890G>C GRCh38
NC_000023.10:g.25023007G>C , CM000685.1:g.25023007G>C GRCh37
NC_000023.9:g.24932928G>C NCBI36
NG_008281.1:g.16059C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1469C>G MANE Select ENSP00000368332.4:p.Pro490Arg
ENST00000636885.1:n.57C>G
ENST00000379044.4:c.1469C>G ENSP00000368332.4:p.Pro490Arg
NM_139058.2:c.1469C>G NP_620689.1:p.Pro490Arg
NM_139058.3:c.1469C>G MANE Select NP_620689.1:p.Pro490Arg