Canonical Allele Identifier: CA2420205835
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004590T= , CM000685.2:g.25004590T= GRCh38
NC_000023.10:g.25022707T= , CM000685.1:g.25022707T= GRCh37
NC_000023.9:g.24932628T= NCBI36
NG_008281.1:g.16359A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.*80A= MANE Select ENSP00000368332.4:n.*80A=
ENST00000379044.4:c.*80A= ENSP00000368332.4:n.*80A=
NM_139058.2:c.*80A= NP_620689.1:n.*80A=
NM_139058.3:c.*80A= MANE Select NP_620689.1:n.*80A=