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ClinGen Allele Registry
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Canonical Allele Identifier:
CA213235
Community Standard Title: NM_139058.3(ARX):c.1465del (p.Ala489ProfsTer3)
Gene: ARX
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.25004895del , CM000685.2:g.25004895del
GRCh38
NC_000023.10:g.25023012del , CM000685.1:g.25023012del
GRCh37
NC_000023.9:g.24932933del
NCBI36
NG_008281.1:g.16055del
Transcript Alleles
HGVS
Amino-acid Change
NM_139058.3:c.1465del
MANE Select
NP_620689.1:p.Ala489ProfsTer3
ENST00000379044.5:c.1465del
MANE Select
ENSP00000368332.4:p.Ala489ProfsTer3
NM_139058.2:c.1465del
NP_620689.1:p.Ala489ProfsTer3
ENST00000379044.4:c.1465del
ENSP00000368332.4:p.Ala489ProfsTer3
ENST00000636885.1:n.53del
Search 100 bp 5'
Search 100 bp 3'