Canonical Allele Identifier: CA2420209079
Gene: ARX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25012996G= , CM000685.2:g.25012996G= GRCh38
NC_000023.10:g.25031113G= , CM000685.1:g.25031113G= GRCh37
NC_000023.9:g.24941034G= NCBI36
NG_008281.1:g.7953C=

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.999C= MANE Select ENSP00000368332.4:p.Thr333=
ENST00000379044.4:c.999C= ENSP00000368332.4:p.Thr333=
NM_139058.2:c.999C= NP_620689.1:p.Thr333=
NM_139058.3:c.999C= MANE Select NP_620689.1:p.Thr333=