Canonical Allele Identifier: CA2420209236
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013366C= , CM000685.2:g.25013366C= GRCh38
NC_000023.10:g.25031483C= , CM000685.1:g.25031483C= GRCh37
NC_000023.9:g.24941404C= NCBI36
NG_008281.1:g.7583G=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.629G= MANE Select ENSP00000368332.4:p.Gly210=
ENST00000379044.4:c.629G= ENSP00000368332.4:p.Gly210=
NM_139058.2:c.629G= NP_620689.1:p.Gly210=
NM_139058.3:c.629G= MANE Select NP_620689.1:p.Gly210=