Canonical Allele Identifier: CA2420207998
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010191A= , CM000685.2:g.25010191A= GRCh38
NC_000023.10:g.25028308A= , CM000685.1:g.25028308A= GRCh37
NC_000023.9:g.24938229A= NCBI36
NG_008281.1:g.10758T=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+69T= MANE Select ENSP00000368332.4:n.1119+69T=
ENST00000379044.4:c.1119+69T= ENSP00000368332.4:n.1119+69T=
NM_139058.2:c.1119+69T= NP_620689.1:n.1119+69T=
NM_139058.3:c.1119+69T= MANE Select NP_620689.1:n.1119+69T=