Canonical Allele Identifier: CA412610975
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25004906-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25004906A>G , CM000685.2:g.25004906A>G GRCh38
NC_000023.10:g.25023023A>G , CM000685.1:g.25023023A>G GRCh37
NC_000023.9:g.24932944A>G NCBI36
NG_008281.1:g.16043T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1453T>C MANE Select ENSP00000368332.4:p.Phe485Leu
ENST00000636885.1:n.41T>C
ENST00000379044.4:c.1453T>C ENSP00000368332.4:p.Phe485Leu
NM_139058.2:c.1453T>C NP_620689.1:p.Phe485Leu
NM_139058.3:c.1453T>C MANE Select NP_620689.1:p.Phe485Leu