Canonical Allele Identifier: CA2420208961
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012755T= , CM000685.2:g.25012755T= GRCh38
NC_000023.10:g.25030872T= , CM000685.1:g.25030872T= GRCh37
NC_000023.9:g.24940793T= NCBI36
NG_008281.1:g.8194A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1073+167A= MANE Select ENSP00000368332.4:n.1073+167A=
ENST00000379044.4:c.1073+167A= ENSP00000368332.4:n.1073+167A=
NM_139058.2:c.1073+167A= NP_620689.1:n.1073+167A=
NM_139058.3:c.1073+167A= MANE Select NP_620689.1:n.1073+167A=