Canonical Allele Identifier: CA2420206898
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25006870A= , CM000685.2:g.25006870A= GRCh38
NC_000023.10:g.25024987A= , CM000685.1:g.25024987A= GRCh37
NC_000023.9:g.24934908A= NCBI36
NG_008281.1:g.14079T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1448+241T= MANE Select ENSP00000368332.4:n.1448+241T=
ENST00000637993.1:c.61+241T=
ENST00000379044.4:c.1448+241T= ENSP00000368332.4:n.1448+241T=
NM_139058.2:c.1448+241T= NP_620689.1:n.1448+241T=
NM_139058.3:c.1448+241T= MANE Select NP_620689.1:n.1448+241T=