Canonical Allele Identifier: CA2420209080
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012997G= , CM000685.2:g.25012997G= GRCh38
NC_000023.10:g.25031114G= , CM000685.1:g.25031114G= GRCh37
NC_000023.9:g.24941035G= NCBI36
NG_008281.1:g.7952C=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.998C= MANE Select ENSP00000368332.4:p.Thr333=
ENST00000379044.4:c.998C= ENSP00000368332.4:p.Thr333=
NM_139058.2:c.998C= NP_620689.1:p.Thr333=
NM_139058.3:c.998C= MANE Select NP_620689.1:p.Thr333=