Canonical Allele Identifier: CA388876500

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21878071T>A (hg19) ; chr14:g.21409912T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21409912T>A , CM000676.2:g.21409912T>A	GRCh38
NC_000014.8:g.21878071T>A , CM000676.1:g.21878071T>A	GRCh37
NC_000014.7:g.20947911T>A	NCBI36
NG_021249.1:g.32387A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1466A>T	ENSP00000406288.3:p.Asp489Val
ENST00000555962.6:c.-110-6870A>T	ENSP00000495174.1:n.-110-6870A>T
ENST00000557364.6:c.2303A>T	ENSP00000451601.1:p.Asp768Val
ENST00000643469.1:c.2303A>T	ENSP00000495070.1:p.Asp768Val
ENST00000645140.1:c.2215A>T
ENST00000645206.1:n.817A>T
ENST00000645929.1:c.1466A>T	ENSP00000494402.1:p.Asp489Val
ENST00000646340.1:c.2309A>T	ENSP00000496730.1:p.Asp770Val
ENST00000646647.2:c.2303A>T MANE Select	ENSP00000495240.1:p.Asp768Val
ENST00000399982.6:c.2303A>T	ENSP00000382863.2:p.Asp768Val
ENST00000430710.7:c.1466A>T	ENSP00000406288.3:p.Asp489Val
ENST00000554384.1:n.171A>T
ENST00000555962.5:n.151-6870A>T
ENST00000557364.5:c.2303A>T	ENSP00000451601.1:p.Asp768Val
NM_001170629.1:c.2303A>T	NP_001164100.1:p.Asp768Val
NM_020920.3:c.1466A>T	NP_065971.2:p.Asp489Val
NM_001170629.2:c.2303A>T MANE Select	NP_001164100.1:p.Asp768Val
NM_020920.4:c.1466A>T	NP_065971.2:p.Asp489Val