Canonical Allele Identifier: CA412612553
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013267A>T , CM000685.2:g.25013267A>T GRCh38
NC_000023.10:g.25031384A>T , CM000685.1:g.25031384A>T GRCh37
NC_000023.9:g.24941305A>T NCBI36
NG_008281.1:g.7682T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.728T>A MANE Select ENSP00000368332.4:p.Leu243Gln
ENST00000379044.4:c.728T>A ENSP00000368332.4:p.Leu243Gln
NM_139058.2:c.728T>A NP_620689.1:p.Leu243Gln
NM_139058.3:c.728T>A MANE Select NP_620689.1:p.Leu243Gln