Canonical Allele Identifier: CA412612001
Gene: ARX HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013004A>C , CM000685.2:g.25013004A>C GRCh38
NC_000023.10:g.25031121A>C , CM000685.1:g.25031121A>C GRCh37
NC_000023.9:g.24941042A>C NCBI36
NG_008281.1:g.7945T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000379044.5:c.991T>G MANE Select ENSP00000368332.4:p.Tyr331Asp
ENST00000379044.4:c.991T>G ENSP00000368332.4:p.Tyr331Asp
NM_139058.2:c.991T>G NP_620689.1:p.Tyr331Asp
NM_139058.3:c.991T>G MANE Select NP_620689.1:p.Tyr331Asp