Canonical Allele Identifier: CA388884663

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21897212A>C (hg19) ; chr14:g.21429053A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429053A>C , CM000676.2:g.21429053A>C	GRCh38
NC_000014.8:g.21897212A>C , CM000676.1:g.21897212A>C	GRCh37
NC_000014.7:g.20967052A>C	NCBI36
NG_021249.1:g.13246T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.289T>G	ENSP00000406288.3:p.Ser97Ala
ENST00000553651.2:n.2932T>G
ENST00000555962.6:c.-111+2758T>G	ENSP00000495174.1:n.-111+2758T>G
ENST00000557364.6:c.1126T>G	ENSP00000451601.1:p.Ser376Ala
ENST00000642518.1:c.289T>G	ENSP00000496722.1:p.Ser97Ala
ENST00000643048.1:n.1421T>G
ENST00000643469.1:c.1126T>G	ENSP00000495070.1:p.Ser376Ala
ENST00000645140.1:c.1038T>G
ENST00000645929.1:c.289T>G	ENSP00000494402.1:p.Ser97Ala
ENST00000646063.1:c.1213T>G	ENSP00000496565.1:p.Ser405Ala
ENST00000646340.1:c.1132T>G	ENSP00000496730.1:p.Ser378Ala
ENST00000646647.2:c.1126T>G MANE Select	ENSP00000495240.1:p.Ser376Ala
ENST00000399982.6:c.1126T>G	ENSP00000382863.2:p.Ser376Ala
ENST00000430710.7:c.289T>G	ENSP00000406288.3:p.Ser97Ala
ENST00000555962.5:n.150+2758T>G
ENST00000557364.5:c.1126T>G	ENSP00000451601.1:p.Ser376Ala
NM_001170629.1:c.1126T>G	NP_001164100.1:p.Ser376Ala
NM_020920.3:c.289T>G	NP_065971.2:p.Ser97Ala
NM_001170629.2:c.1126T>G MANE Select	NP_001164100.1:p.Ser376Ala
NM_020920.4:c.289T>G	NP_065971.2:p.Ser97Ala