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ClinGen Allele Registry
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Canonical Allele Identifier:
CA2420208034
Community Standard Title: NM_139058.3(ARX):c.1111C= (p.Arg371=)
Gene: ARX
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.25010268G= , CM000685.2:g.25010268G=
GRCh38
NC_000023.10:g.25028385G= , CM000685.1:g.25028385G=
GRCh37
NC_000023.9:g.24938306G=
NCBI36
NG_008281.1:g.10681C=
Transcript Alleles
HGVS
Amino-acid Change
NM_139058.3:c.1111C=
MANE Select
NP_620689.1:p.Arg371=
ENST00000379044.5:c.1111C=
MANE Select
ENSP00000368332.4:p.Arg371=
NM_139058.2:c.1111C=
NP_620689.1:p.Arg371=
ENST00000379044.4:c.1111C=
ENSP00000368332.4:p.Arg371=
Search 100 bp 5'
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