Canonical Allele Identifier: CA2420209054
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012918A= , CM000685.2:g.25012918A= GRCh38
NC_000023.10:g.25031035A= , CM000685.1:g.25031035A= GRCh37
NC_000023.9:g.24940956A= NCBI36
NG_008281.1:g.8031T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1073+4T= MANE Select ENSP00000368332.4:n.1073+4T=
ENST00000379044.4:c.1073+4T= ENSP00000368332.4:n.1073+4T=
NM_139058.2:c.1073+4T= NP_620689.1:n.1073+4T=
NM_139058.3:c.1073+4T= MANE Select NP_620689.1:n.1073+4T=