Canonical Allele Identifier: CA163342
Gene: ADNP HGNC NCBI

Linked Data

ClinVar Variation Id: 139632
ClinVar RCV Id: RCV002312954
dbSNP Id: rs587777523

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.50892219_50892222del , CM000682.2:g.50892219_50892222del GRCh38
NC_000020.10:g.49508756_49508759del , CM000682.1:g.49508756_49508759del GRCh37
NC_000020.9:g.48942163_48942166del NCBI36
NG_034200.1:g.43773_43776del

Transcript Alleles

HGVS Amino-acid change
ENST00000349014.8:c.2496_2499del ENSP00000342905.3:p.Asn832LysfsTer?
ENST00000371602.9:c.2496_2499del ENSP00000360662.2:p.Asn832LysfsTer?
ENST00000396029.8:c.2496_2499del ENSP00000379346.3:p.Asn832LysfsTer?
ENST00000396032.8:c.2496_2499del ENSP00000379349.2:p.Asn832LysfsTer?
ENST00000621696.5:c.2496_2499del MANE Select ENSP00000483881.1:p.Asn832LysfsTer?
ENST00000644386.1:c.202-2261_202-2258del ENSP00000493755.1:n.202-2261_202-2258del
ENST00000645081.1:c.1812_1815del ENSP00000495540.1:p.Asn604LysfsTer?
ENST00000673732.1:c.2712_2715del ENSP00000501294.1:p.Asn904LysfsTer?
ENST00000349014.7:c.2496_2499del ENSP00000342905.3:p.Asn832LysfsTer?
ENST00000371602.8:c.2496_2499del ENSP00000360662.2:p.Asn832LysfsTer?
ENST00000396029.7:c.2496_2499del ENSP00000379346.3:p.Asn832LysfsTer?
ENST00000396032.7:c.2496_2499del ENSP00000379349.2:p.Asn832LysfsTer?
ENST00000621696.4:c.2496_2499del ENSP00000483881.1:p.Asn832LysfsTer?
NM_001282531.1:c.2496_2499del NP_001269460.1:p.Asn832LysfsTer?
NM_001282532.1:c.2496_2499del NP_001269461.1:p.Asn832LysfsTer?
NM_015339.3:c.2496_2499del NP_056154.1:p.Asn832LysfsTer?
NM_181442.2:c.2496_2499del NP_852107.1:p.Asn832LysfsTer?
XM_011528747.1:c.2496_2499del XP_011527049.1:p.Asn832LysfsTer?
XM_011528748.1:c.2523_2526del XP_011527050.1:p.Asn841LysfsTer?
NM_001282531.2:c.2496_2499del NP_001269460.1:p.Asn832LysfsTer?
NM_001347511.1:c.2496_2499del NP_001334440.1:p.Asn832LysfsTer?
NM_015339.4:c.2496_2499del NP_056154.1:p.Asn832LysfsTer?
NM_181442.3:c.2496_2499del NP_852107.1:p.Asn832LysfsTer?
XM_011528747.2:c.2496_2499del XP_011527049.1:p.Asn832LysfsTer?
XM_011528748.2:c.2523_2526del XP_011527050.1:p.Asn841LysfsTer?
XM_017027758.1:c.2496_2499del XP_016883247.1:p.Asn832LysfsTer?
XM_017027759.1:c.2496_2499del XP_016883248.1:p.Asn832LysfsTer?
NM_001282531.3:c.2496_2499del MANE Select NP_001269460.1:p.Asn832LysfsTer?
NM_001347511.2:c.2496_2499del NP_001334440.1:p.Asn832LysfsTer?
NM_015339.5:c.2496_2499del NP_056154.1:p.Asn832LysfsTer?
NM_181442.4:c.2496_2499del NP_852107.1:p.Asn832LysfsTer?
NM_001282532.2:c.2496_2499del NP_001269461.1:p.Asn832LysfsTer?