Canonical Allele Identifier: CA388893678

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21868642A>C (hg19) ; chr14:g.21400483A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21400483A>C , CM000676.2:g.21400483A>C	GRCh38
NC_000014.8:g.21868642A>C , CM000676.1:g.21868642A>C	GRCh37
NC_000014.7:g.20938482A>C	NCBI36
NG_021249.1:g.41816T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.3663T>G	ENSP00000406288.3:p.Ile1221Met
ENST00000555935.2:c.2176T>G
ENST00000555962.6:c.265-176T>G	ENSP00000495174.1:n.265-176T>G
ENST00000557364.6:c.4500T>G	ENSP00000451601.1:p.Ile1500Met
ENST00000643469.1:c.4500T>G	ENSP00000495070.1:p.Ile1500Met
ENST00000645206.1:n.3014T>G
ENST00000645929.1:c.3663T>G	ENSP00000494402.1:p.Ile1221Met
ENST00000646340.1:c.4506T>G	ENSP00000496730.1:p.Ile1502Met
ENST00000646558.1:n.1316T>G
ENST00000646647.2:c.4500T>G MANE Select	ENSP00000495240.1:p.Ile1500Met
ENST00000399982.6:c.4500T>G	ENSP00000382863.2:p.Ile1500Met
ENST00000430710.7:c.3663T>G	ENSP00000406288.3:p.Ile1221Met
ENST00000555935.1:c.2176T>G
ENST00000555962.5:n.525-176T>G
ENST00000557364.5:c.4500T>G	ENSP00000451601.1:p.Ile1500Met
NM_001170629.1:c.4500T>G	NP_001164100.1:p.Ile1500Met
NM_020920.3:c.3663T>G	NP_065971.2:p.Ile1221Met
NM_001170629.2:c.4500T>G MANE Select	NP_001164100.1:p.Ile1500Met
NM_020920.4:c.3663T>G	NP_065971.2:p.Ile1221Met