Canonical Allele Identifier: CA2573157170
Gene: ADNP HGNC NCBI

Linked Data

ClinVar Variation Id: 1527880
ClinVar RCV Id: RCV002077361
dbSNP Id: rs2122746230

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.50892548del , CM000682.2:g.50892548del GRCh38
NC_000020.10:g.49509085del , CM000682.1:g.49509085del GRCh37
NC_000020.9:g.48942492del NCBI36
NG_034200.1:g.43444del

Transcript Alleles

HGVS Amino-acid Change
ENST00000349014.8:c.2167del ENSP00000342905.3:p.Glu723AsnfsTer5
ENST00000371602.9:c.2167del ENSP00000360662.2:p.Glu723AsnfsTer5
ENST00000396029.8:c.2167del ENSP00000379346.3:p.Glu723AsnfsTer5
ENST00000396032.8:c.2167del ENSP00000379349.2:p.Glu723AsnfsTer5
ENST00000621696.5:c.2167del MANE Select ENSP00000483881.1:p.Glu723AsnfsTer5
ENST00000644386.1:c.202-2590del ENSP00000493755.1:n.202-2590del
ENST00000645081.1:c.1483del ENSP00000495540.1:p.Glu495AsnfsTer5
ENST00000673732.1:c.2383del ENSP00000501294.1:p.Glu795AsnfsTer5
ENST00000349014.7:c.2167del ENSP00000342905.3:p.Glu723AsnfsTer5
ENST00000371602.8:c.2167del ENSP00000360662.2:p.Glu723AsnfsTer5
ENST00000396029.7:c.2167del ENSP00000379346.3:p.Glu723AsnfsTer5
ENST00000396032.7:c.2167del ENSP00000379349.2:p.Glu723AsnfsTer5
ENST00000621696.4:c.2167del ENSP00000483881.1:p.Glu723AsnfsTer5
NM_001282531.1:c.2167del NP_001269460.1:p.Glu723AsnfsTer5
NM_001282532.1:c.2167del NP_001269461.1:p.Glu723AsnfsTer5
NM_015339.3:c.2167del NP_056154.1:p.Glu723AsnfsTer5
NM_181442.2:c.2167del NP_852107.1:p.Glu723AsnfsTer5
XM_011528747.1:c.2167del XP_011527049.1:p.Glu723AsnfsTer5
XM_011528748.1:c.2194del XP_011527050.1:p.Glu732AsnfsTer5
NM_001282531.2:c.2167del NP_001269460.1:p.Glu723AsnfsTer5
NM_001347511.1:c.2167del NP_001334440.1:p.Glu723AsnfsTer5
NM_015339.4:c.2167del NP_056154.1:p.Glu723AsnfsTer5
NM_181442.3:c.2167del NP_852107.1:p.Glu723AsnfsTer5
XM_011528747.2:c.2167del XP_011527049.1:p.Glu723AsnfsTer5
XM_011528748.2:c.2194del XP_011527050.1:p.Glu732AsnfsTer5
XM_017027758.1:c.2167del XP_016883247.1:p.Glu723AsnfsTer5
XM_017027759.1:c.2167del XP_016883248.1:p.Glu723AsnfsTer5
NM_001282531.3:c.2167del MANE Select NP_001269460.1:p.Glu723AsnfsTer5
NM_001347511.2:c.2167del NP_001334440.1:p.Glu723AsnfsTer5
NM_015339.5:c.2167del NP_056154.1:p.Glu723AsnfsTer5
NM_181442.4:c.2167del NP_852107.1:p.Glu723AsnfsTer5
NM_001282532.2:c.2167del NP_001269461.1:p.Glu723AsnfsTer5