Canonical Allele Identifier: CA388876376
Gene: CHD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21409855C>G , CM000676.2:g.21409855C>G GRCh38
NC_000014.8:g.21878014C>G , CM000676.1:g.21878014C>G GRCh37
NC_000014.7:g.20947854C>G NCBI36
NG_021249.1:g.32444G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.1523G>C ENSP00000406288.3:p.Arg508Thr
ENST00000555935.2:c.36G>C
ENST00000555962.6:c.-110-6813G>C ENSP00000495174.1:n.-110-6813G>C
ENST00000557364.6:c.2360G>C ENSP00000451601.1:p.Arg787Thr
ENST00000643469.1:c.2360G>C ENSP00000495070.1:p.Arg787Thr
ENST00000645140.1:c.2272G>C
ENST00000645206.1:n.874G>C
ENST00000645929.1:c.1523G>C ENSP00000494402.1:p.Arg508Thr
ENST00000646340.1:c.2366G>C ENSP00000496730.1:p.Arg789Thr
ENST00000646647.2:c.2360G>C MANE Select ENSP00000495240.1:p.Arg787Thr
ENST00000399982.6:c.2360G>C ENSP00000382863.2:p.Arg787Thr
ENST00000430710.7:c.1523G>C ENSP00000406288.3:p.Arg508Thr
ENST00000554384.1:n.228G>C
ENST00000555935.1:c.36G>C
ENST00000555962.5:n.151-6813G>C
ENST00000557364.5:c.2360G>C ENSP00000451601.1:p.Arg787Thr
NM_001170629.1:c.2360G>C NP_001164100.1:p.Arg787Thr
NM_020920.3:c.1523G>C NP_065971.2:p.Arg508Thr
NM_001170629.2:c.2360G>C MANE Select NP_001164100.1:p.Arg787Thr
NM_020920.4:c.1523G>C NP_065971.2:p.Arg508Thr