Canonical Allele Identifier: CA412611773
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25010291A>T , CM000685.2:g.25010291A>T GRCh38
NC_000023.10:g.25028408A>T , CM000685.1:g.25028408A>T GRCh37
NC_000023.9:g.24938329A>T NCBI36
NG_008281.1:g.10658T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.1088T>A MANE Select ENSP00000368332.4:p.Met363Lys
ENST00000379044.4:c.1088T>A ENSP00000368332.4:p.Met363Lys
NM_139058.2:c.1088T>A NP_620689.1:p.Met363Lys
NM_139058.3:c.1088T>A MANE Select NP_620689.1:p.Met363Lys