Canonical Allele Identifier: CA2420205826
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004566C= , CM000685.2:g.25004566C= GRCh38
NC_000023.10:g.25022683C= , CM000685.1:g.25022683C= GRCh37
NC_000023.9:g.24932604C= NCBI36
NG_008281.1:g.16383G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.*104G= MANE Select ENSP00000368332.4:n.*104G=
ENST00000379044.4:c.*104G= ENSP00000368332.4:n.*104G=
NM_139058.2:c.*104G= NP_620689.1:n.*104G=
NM_139058.3:c.*104G= MANE Select NP_620689.1:n.*104G=