Canonical Allele Identifier: CA2420206889
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25006840G= , CM000685.2:g.25006840G= GRCh38
NC_000023.10:g.25024957G= , CM000685.1:g.25024957G= GRCh37
NC_000023.9:g.24934878G= NCBI36
NG_008281.1:g.14109C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1448+271C= MANE Select ENSP00000368332.4:n.1448+271C=
ENST00000637993.1:c.62-213C=
ENST00000379044.4:c.1448+271C= ENSP00000368332.4:n.1448+271C=
NM_139058.2:c.1448+271C= NP_620689.1:n.1448+271C=
NM_139058.3:c.1448+271C= MANE Select NP_620689.1:n.1448+271C=