Canonical Allele Identifier: CA485000767

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21868642A>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.3663T>C	ENSP00000406288.3:p.Ile1221=
ENST00000555935.2:c.2176T>C
ENST00000555962.6:c.265-176T>C	ENSP00000495174.1:n.265-176T>C
ENST00000557364.6:c.4500T>C	ENSP00000451601.1:p.Ile1500=
ENST00000643469.1:c.4500T>C	ENSP00000495070.1:p.Ile1500=
ENST00000645206.1:n.3014T>C
ENST00000645929.1:c.3663T>C	ENSP00000494402.1:p.Ile1221=
ENST00000646340.1:c.4506T>C	ENSP00000496730.1:p.Ile1502=
ENST00000646558.1:n.1316T>C
ENST00000646647.2:c.4500T>C MANE Select	ENSP00000495240.1:p.Ile1500=
ENST00000399982.6:c.4500T>C	ENSP00000382863.2:p.Ile1500=
ENST00000430710.7:c.3663T>C	ENSP00000406288.3:p.Ile1221=
ENST00000555935.1:c.2176T>C
ENST00000555962.5:n.525-176T>C
ENST00000557364.5:c.4500T>C	ENSP00000451601.1:p.Ile1500=
NM_001170629.1:c.4500T>C	NP_001164100.1:p.Ile1500=
NM_020920.3:c.3663T>C	NP_065971.2:p.Ile1221=
NM_001170629.2:c.4500T>C MANE Select	NP_001164100.1:p.Ile1500=
NM_020920.4:c.3663T>C	NP_065971.2:p.Ile1221=