Canonical Allele Identifier: CA408967501
Community Standard Title: NM_001282531.3(ADNP):c.2919G>C (p.Glu973Asp)
Gene: ADNP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.50891795C>G , CM000682.2:g.50891795C>G GRCh38
NC_000020.10:g.49508332C>G , CM000682.1:g.49508332C>G GRCh37
NC_000020.9:g.48941739C>G NCBI36
NG_034200.1:g.44196G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001282531.3:c.2919G>C MANE Select NP_001269460.1:p.Glu973Asp
ENST00000621696.5:c.2919G>C MANE Select ENSP00000483881.1:p.Glu973Asp
NM_001282531.1:c.2919G>C NP_001269460.1:p.Glu973Asp
NM_001282531.2:c.2919G>C NP_001269460.1:p.Glu973Asp
NM_001282532.1:c.2919G>C NP_001269461.1:p.Glu973Asp
NM_001282532.2:c.2919G>C NP_001269461.1:p.Glu973Asp
NM_001347511.1:c.2919G>C NP_001334440.1:p.Glu973Asp
NM_001347511.2:c.2919G>C NP_001334440.1:p.Glu973Asp
NM_015339.3:c.2919G>C NP_056154.1:p.Glu973Asp
NM_015339.4:c.2919G>C NP_056154.1:p.Glu973Asp
NM_015339.5:c.2919G>C NP_056154.1:p.Glu973Asp
NM_181442.2:c.2919G>C NP_852107.1:p.Glu973Asp
NM_181442.3:c.2919G>C NP_852107.1:p.Glu973Asp
NM_181442.4:c.2919G>C NP_852107.1:p.Glu973Asp
ENST00000349014.7:c.2919G>C ENSP00000342905.3:p.Glu973Asp
ENST00000349014.8:c.2919G>C ENSP00000342905.3:p.Glu973Asp
ENST00000371602.8:c.2919G>C ENSP00000360662.2:p.Glu973Asp
ENST00000371602.9:c.2919G>C ENSP00000360662.2:p.Glu973Asp
ENST00000396029.7:c.2919G>C ENSP00000379346.3:p.Glu973Asp
ENST00000396029.8:c.2919G>C ENSP00000379346.3:p.Glu973Asp
ENST00000396032.7:c.2919G>C ENSP00000379349.2:p.Glu973Asp
ENST00000396032.8:c.2919G>C ENSP00000379349.2:p.Glu973Asp
ENST00000621696.4:c.2919G>C ENSP00000483881.1:p.Glu973Asp
ENST00000644386.1:c.202-1838G>C ENSP00000493755.1:n.202-1838G>C
ENST00000645081.1:c.2235G>C ENSP00000495540.1:p.Glu745Asp
ENST00000673732.1:c.3135G>C ENSP00000501294.1:p.Glu1045Asp
XM_011528747.1:c.2919G>C XP_011527049.1:p.Glu973Asp
XM_011528747.2:c.2919G>C XP_011527049.1:p.Glu973Asp
XM_011528748.1:c.2946G>C XP_011527050.1:p.Glu982Asp
XM_011528748.2:c.2946G>C XP_011527050.1:p.Glu982Asp
XM_017027758.1:c.2919G>C XP_016883247.1:p.Glu973Asp
XM_017027759.1:c.2919G>C XP_016883248.1:p.Glu973Asp