Canonical Allele Identifier: CA408974864

Gene: ADNP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.50893738G>C , CM000682.2:g.50893738G>C	GRCh38
NC_000020.10:g.49510275G>C , CM000682.1:g.49510275G>C	GRCh37
NC_000020.9:g.48943682G>C	NCBI36
NG_034200.1:g.42253C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001282531.3:c.976C>G MANE Select	NP_001269460.1:p.His326Asp
ENST00000621696.5:c.976C>G MANE Select	ENSP00000483881.1:p.His326Asp
NM_001282531.1:c.976C>G	NP_001269460.1:p.His326Asp
NM_001282531.2:c.976C>G	NP_001269460.1:p.His326Asp
NM_001282532.1:c.976C>G	NP_001269461.1:p.His326Asp
NM_001282532.2:c.976C>G	NP_001269461.1:p.His326Asp
NM_001347511.1:c.976C>G	NP_001334440.1:p.His326Asp
NM_001347511.2:c.976C>G	NP_001334440.1:p.His326Asp
NM_015339.3:c.976C>G	NP_056154.1:p.His326Asp
NM_015339.4:c.976C>G	NP_056154.1:p.His326Asp
NM_015339.5:c.976C>G	NP_056154.1:p.His326Asp
NM_181442.2:c.976C>G	NP_852107.1:p.His326Asp
NM_181442.3:c.976C>G	NP_852107.1:p.His326Asp
NM_181442.4:c.976C>G	NP_852107.1:p.His326Asp
ENST00000349014.7:c.976C>G	ENSP00000342905.3:p.His326Asp
ENST00000349014.8:c.976C>G	ENSP00000342905.3:p.His326Asp
ENST00000371602.8:c.976C>G	ENSP00000360662.2:p.His326Asp
ENST00000371602.9:c.976C>G	ENSP00000360662.2:p.His326Asp
ENST00000396029.7:c.976C>G	ENSP00000379346.3:p.His326Asp
ENST00000396029.8:c.976C>G	ENSP00000379346.3:p.His326Asp
ENST00000396032.7:c.976C>G	ENSP00000379349.2:p.His326Asp
ENST00000396032.8:c.976C>G	ENSP00000379349.2:p.His326Asp
ENST00000621696.4:c.976C>G	ENSP00000483881.1:p.His326Asp
ENST00000644386.1:c.202-3781C>G	ENSP00000493755.1:n.202-3781C>G
ENST00000645081.1:c.292C>G	ENSP00000495540.1:p.His98Asp
ENST00000673732.1:c.1192C>G	ENSP00000501294.1:p.His398Asp
XM_011528747.1:c.976C>G	XP_011527049.1:p.His326Asp
XM_011528747.2:c.976C>G	XP_011527049.1:p.His326Asp
XM_011528748.1:c.1003C>G	XP_011527050.1:p.His335Asp
XM_011528748.2:c.1003C>G	XP_011527050.1:p.His335Asp
XM_017027758.1:c.976C>G	XP_016883247.1:p.His326Asp
XM_017027759.1:c.976C>G	XP_016883248.1:p.His326Asp