Canonical Allele Identifier: CA2420207047
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25007236G= , CM000685.2:g.25007236G= GRCh38
NC_000023.10:g.25025353G= , CM000685.1:g.25025353G= GRCh37
NC_000023.9:g.24935274G= NCBI36
NG_008281.1:g.13713C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1323C= MANE Select ENSP00000368332.4:p.Phe441=
ENST00000379044.4:c.1323C= ENSP00000368332.4:p.Phe441=
NM_139058.2:c.1323C= NP_620689.1:p.Phe441=
NM_139058.3:c.1323C= MANE Select NP_620689.1:p.Phe441=