Canonical Allele Identifier: CA1139666744
Gene: ADNP HGNC NCBI

Linked Data

ClinVar Variation Id: 973033
ClinVar RCV Id: RCV001249371
dbSNP Id: rs1982227129

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.50903914_50903917del , CM000682.2:g.50903914_50903917del GRCh38
NC_000020.10:g.49520451_49520454del , CM000682.1:g.49520451_49520454del GRCh37
NC_000020.9:g.48953858_48953861del NCBI36
NG_034200.1:g.32076_32079del

Transcript Alleles

HGVS Amino-acid Change
ENST00000349014.8:c.82_85del ENSP00000342905.3:p.Leu28AsnfsTer7
ENST00000371602.9:c.82_85del ENSP00000360662.2:p.Leu28AsnfsTer7
ENST00000396029.8:c.82_85del ENSP00000379346.3:p.Leu28AsnfsTer7
ENST00000396032.8:c.82_85del ENSP00000379349.2:p.Leu28AsnfsTer7
ENST00000621696.5:c.82_85del MANE Select ENSP00000483881.1:p.Leu28AsnfsTer7
ENST00000642364.1:n.86-1806_86-1803del
ENST00000644386.1:c.82_85del ENSP00000493755.1:p.Leu28AsnfsTer7
ENST00000645081.1:c.-576-1806_-576-1803del ENSP00000495540.1:n.-576-1806_-576-1803del
ENST00000673732.1:c.298_301del ENSP00000501294.1:p.Leu100AsnfsTer7
ENST00000349014.7:c.82_85del ENSP00000342905.3:p.Leu28AsnfsTer7
ENST00000371602.8:c.82_85del ENSP00000360662.2:p.Leu28AsnfsTer7
ENST00000396029.7:c.82_85del ENSP00000379346.3:p.Leu28AsnfsTer7
ENST00000396032.7:c.82_85del ENSP00000379349.2:p.Leu28AsnfsTer7
ENST00000534467.1:c.82_85del ENSP00000436181.1:p.Leu28AsnfsTer7
ENST00000621696.4:c.82_85del ENSP00000483881.1:p.Leu28AsnfsTer7
NM_001282531.1:c.82_85del NP_001269460.1:p.Leu28AsnfsTer7
NM_001282532.1:c.82_85del NP_001269461.1:p.Leu28AsnfsTer7
NM_015339.3:c.82_85del NP_056154.1:p.Leu28AsnfsTer7
NM_181442.2:c.82_85del NP_852107.1:p.Leu28AsnfsTer7
XM_011528747.1:c.82_85del XP_011527049.1:p.Leu28AsnfsTer7
XM_011528748.1:c.109_112del XP_011527050.1:p.Leu37AsnfsTer7
NM_001282531.2:c.82_85del NP_001269460.1:p.Leu28AsnfsTer7
NM_001347511.1:c.82_85del NP_001334440.1:p.Leu28AsnfsTer7
NM_015339.4:c.82_85del NP_056154.1:p.Leu28AsnfsTer7
NM_181442.3:c.82_85del NP_852107.1:p.Leu28AsnfsTer7
XM_011528747.2:c.82_85del XP_011527049.1:p.Leu28AsnfsTer7
XM_011528748.2:c.109_112del XP_011527050.1:p.Leu37AsnfsTer7
XM_017027758.1:c.82_85del XP_016883247.1:p.Leu28AsnfsTer7
XM_017027759.1:c.82_85del XP_016883248.1:p.Leu28AsnfsTer7
NM_001282531.3:c.82_85del MANE Select NP_001269460.1:p.Leu28AsnfsTer7
NM_001347511.2:c.82_85del NP_001334440.1:p.Leu28AsnfsTer7
NM_015339.5:c.82_85del NP_056154.1:p.Leu28AsnfsTer7
NM_181442.4:c.82_85del NP_852107.1:p.Leu28AsnfsTer7
NM_001282532.2:c.82_85del NP_001269461.1:p.Leu28AsnfsTer7