Canonical Allele Identifier: CA2420207974
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010154T= , CM000685.2:g.25010154T= GRCh38
NC_000023.10:g.25028271T= , CM000685.1:g.25028271T= GRCh37
NC_000023.9:g.24938192T= NCBI36
NG_008281.1:g.10795A=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1119+106A= MANE Select ENSP00000368332.4:n.1119+106A=
ENST00000379044.4:c.1119+106A= ENSP00000368332.4:n.1119+106A=
NM_139058.2:c.1119+106A= NP_620689.1:n.1119+106A=
NM_139058.3:c.1119+106A= MANE Select NP_620689.1:n.1119+106A=