Canonical Allele Identifier: CA2420209075
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012981G= , CM000685.2:g.25012981G= GRCh38
NC_000023.10:g.25031098G= , CM000685.1:g.25031098G= GRCh37
NC_000023.9:g.24941019G= NCBI36
NG_008281.1:g.7968C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1014C= MANE Select ENSP00000368332.4:p.Tyr338=
ENST00000379044.4:c.1014C= ENSP00000368332.4:p.Tyr338=
NM_139058.2:c.1014C= NP_620689.1:p.Tyr338=
NM_139058.3:c.1014C= MANE Select NP_620689.1:p.Tyr338=