Canonical Allele Identifier: CA2693353372
Gene: ARX HGNC NCBI

Linked Data

gnomAD v4: X-25007451-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25007451A>T , CM000685.2:g.25007451A>T GRCh38
NC_000023.10:g.25025568A>T , CM000685.1:g.25025568A>T GRCh37
NC_000023.9:g.24935489A>T NCBI36
NG_008281.1:g.13498T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.1120-12T>A MANE Select ENSP00000368332.4:n.1120-12T>A
ENST00000379044.4:c.1120-12T>A ENSP00000368332.4:n.1120-12T>A
NM_139058.2:c.1120-12T>A NP_620689.1:n.1120-12T>A
NM_139058.3:c.1120-12T>A MANE Select NP_620689.1:n.1120-12T>A
Search 100 bp 5'
Search 100 bp 3'