Canonical Allele Identifier: CA641006829
Gene: ARX HGNC NCBI

Linked Data

dbSNP Id: rs1266519133
gnomAD v2: X-25031953-CG-C
gnomAD v4: X-25013836-CG-C
MyVariant Identifiers: chrX:g.25031954del (hg19) chrX:g.25013837del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.25013840del , CM000685.2:g.25013840del GRCh38
NC_000023.10:g.25031957del , CM000685.1:g.25031957del GRCh37
NC_000023.9:g.24941878del NCBI36
NG_008281.1:g.7112del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379044.5:c.197-39del MANE Select ENSP00000368332.4:n.197-39del
ENST00000379044.4:c.197-39del ENSP00000368332.4:n.197-39del
NM_139058.2:c.197-39del NP_620689.1:n.197-39del
NM_139058.3:c.197-39del MANE Select NP_620689.1:n.197-39del
Search 100 bp 5'
Search 100 bp 3'