Canonical Allele Identifier: CA388876418

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21878032C>A (hg19) ; chr14:g.21409873C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21409873C>A , CM000676.2:g.21409873C>A	GRCh38
NC_000014.8:g.21878032C>A , CM000676.1:g.21878032C>A	GRCh37
NC_000014.7:g.20947872C>A	NCBI36
NG_021249.1:g.32426G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.1505G>T	ENSP00000406288.3:p.Arg502Met
ENST00000555935.2:c.18G>T
ENST00000555962.6:c.-110-6831G>T	ENSP00000495174.1:n.-110-6831G>T
ENST00000557364.6:c.2342G>T	ENSP00000451601.1:p.Arg781Met
ENST00000643469.1:c.2342G>T	ENSP00000495070.1:p.Arg781Met
ENST00000645140.1:c.2254G>T
ENST00000645206.1:n.856G>T
ENST00000645929.1:c.1505G>T	ENSP00000494402.1:p.Arg502Met
ENST00000646340.1:c.2348G>T	ENSP00000496730.1:p.Arg783Met
ENST00000646647.2:c.2342G>T MANE Select	ENSP00000495240.1:p.Arg781Met
ENST00000399982.6:c.2342G>T	ENSP00000382863.2:p.Arg781Met
ENST00000430710.7:c.1505G>T	ENSP00000406288.3:p.Arg502Met
ENST00000554384.1:n.210G>T
ENST00000555935.1:c.18G>T
ENST00000555962.5:n.151-6831G>T
ENST00000557364.5:c.2342G>T	ENSP00000451601.1:p.Arg781Met
NM_001170629.1:c.2342G>T	NP_001164100.1:p.Arg781Met
NM_020920.3:c.1505G>T	NP_065971.2:p.Arg502Met
NM_001170629.2:c.2342G>T MANE Select	NP_001164100.1:p.Arg781Met
NM_020920.4:c.1505G>T	NP_065971.2:p.Arg502Met