Canonical Allele Identifier: CA2420210087
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25015536C= , CM000685.2:g.25015536C= GRCh38
NC_000023.10:g.25033653C= , CM000685.1:g.25033653C= GRCh37
NC_000023.9:g.24943574C= NCBI36
NG_008281.1:g.5413G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.196+6G= MANE Select ENSP00000368332.4:n.196+6G=
ENST00000379044.4:c.196+6G= ENSP00000368332.4:n.196+6G=
NM_139058.2:c.196+6G= NP_620689.1:n.196+6G=
NM_139058.3:c.196+6G= MANE Select NP_620689.1:n.196+6G=