Canonical Allele Identifier: CA388893572

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21868631A>G (hg19) ; chr14:g.21400472A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21400472A>G , CM000676.2:g.21400472A>G	GRCh38
NC_000014.8:g.21868631A>G , CM000676.1:g.21868631A>G	GRCh37
NC_000014.7:g.20938471A>G	NCBI36
NG_021249.1:g.41827T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.3674T>C	ENSP00000406288.3:p.Ile1225Thr
ENST00000555935.2:c.2187T>C
ENST00000555962.6:c.265-165T>C	ENSP00000495174.1:n.265-165T>C
ENST00000557364.6:c.4511T>C	ENSP00000451601.1:p.Ile1504Thr
ENST00000643469.1:c.4511T>C	ENSP00000495070.1:p.Ile1504Thr
ENST00000645206.1:n.3025T>C
ENST00000645929.1:c.3674T>C	ENSP00000494402.1:p.Ile1225Thr
ENST00000646340.1:c.4517T>C	ENSP00000496730.1:p.Ile1506Thr
ENST00000646558.1:n.1327T>C
ENST00000646647.2:c.4511T>C MANE Select	ENSP00000495240.1:p.Ile1504Thr
ENST00000399982.6:c.4511T>C	ENSP00000382863.2:p.Ile1504Thr
ENST00000430710.7:c.3674T>C	ENSP00000406288.3:p.Ile1225Thr
ENST00000555935.1:c.2187T>C
ENST00000555962.5:n.525-165T>C
ENST00000557364.5:c.4511T>C	ENSP00000451601.1:p.Ile1504Thr
NM_001170629.1:c.4511T>C	NP_001164100.1:p.Ile1504Thr
NM_020920.3:c.3674T>C	NP_065971.2:p.Ile1225Thr
NM_001170629.2:c.4511T>C MANE Select	NP_001164100.1:p.Ile1504Thr
NM_020920.4:c.3674T>C	NP_065971.2:p.Ile1225Thr