Canonical Allele Identifier: CA388879130
Gene: CHD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21415593A>T , CM000676.2:g.21415593A>T GRCh38
NC_000014.8:g.21883752A>T , CM000676.1:g.21883752A>T GRCh37
NC_000014.7:g.20953592A>T NCBI36
NG_021249.1:g.26706T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000430710.8:c.1112T>A ENSP00000406288.3:p.Met371Lys
ENST00000555962.6:c.-110-12551T>A ENSP00000495174.1:n.-110-12551T>A
ENST00000557364.6:c.1949T>A ENSP00000451601.1:p.Met650Lys
ENST00000642914.1:n.932T>A
ENST00000643469.1:c.1949T>A ENSP00000495070.1:p.Met650Lys
ENST00000645140.1:c.1861T>A
ENST00000645206.1:n.463T>A
ENST00000645929.1:c.1112T>A ENSP00000494402.1:p.Met371Lys
ENST00000646340.1:c.1955T>A ENSP00000496730.1:p.Met652Lys
ENST00000646647.2:c.1949T>A MANE Select ENSP00000495240.1:p.Met650Lys
ENST00000399982.6:c.1949T>A ENSP00000382863.2:p.Met650Lys
ENST00000430710.7:c.1112T>A ENSP00000406288.3:p.Met371Lys
ENST00000555962.5:n.151-12551T>A
ENST00000557364.5:c.1949T>A ENSP00000451601.1:p.Met650Lys
NM_001170629.1:c.1949T>A NP_001164100.1:p.Met650Lys
NM_020920.3:c.1112T>A NP_065971.2:p.Met371Lys
NM_001170629.2:c.1949T>A MANE Select NP_001164100.1:p.Met650Lys
NM_020920.4:c.1112T>A NP_065971.2:p.Met371Lys