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ClinGen Allele Registry
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Canonical Allele Identifier:
CA213326
Community Standard Title: NM_139058.3(ARX):c.1096del (p.Asp366ThrfsTer2)
Gene: ARX
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.25010284del , CM000685.2:g.25010284del
GRCh38
NC_000023.10:g.25028401del , CM000685.1:g.25028401del
GRCh37
NC_000023.9:g.24938322del
NCBI36
NG_008281.1:g.10666del
Transcript Alleles
HGVS
Amino-acid Change
NM_139058.3:c.1096del
MANE Select
NP_620689.1:p.Asp366ThrfsTer2
ENST00000379044.5:c.1096del
MANE Select
ENSP00000368332.4:p.Asp366ThrfsTer2
NM_139058.2:c.1096del
NP_620689.1:p.Asp366ThrfsTer2
ENST00000379044.4:c.1096del
ENSP00000368332.4:p.Asp366ThrfsTer2
Search 100 bp 5'
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