Canonical Allele Identifier: CA485000769

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21868645A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21400486A>G , CM000676.2:g.21400486A>G	GRCh38
NC_000014.8:g.21868645A>G , CM000676.1:g.21868645A>G	GRCh37
NC_000014.7:g.20938485A>G	NCBI36
NG_021249.1:g.41813T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.3660T>C	ENSP00000406288.3:p.Asn1220=
ENST00000555935.2:c.2173T>C
ENST00000555962.6:c.265-179T>C	ENSP00000495174.1:n.265-179T>C
ENST00000557364.6:c.4497T>C	ENSP00000451601.1:p.Asn1499=
ENST00000643469.1:c.4497T>C	ENSP00000495070.1:p.Asn1499=
ENST00000645206.1:n.3011T>C
ENST00000645929.1:c.3660T>C	ENSP00000494402.1:p.Asn1220=
ENST00000646340.1:c.4503T>C	ENSP00000496730.1:p.Asn1501=
ENST00000646558.1:n.1313T>C
ENST00000646647.2:c.4497T>C MANE Select	ENSP00000495240.1:p.Asn1499=
ENST00000399982.6:c.4497T>C	ENSP00000382863.2:p.Asn1499=
ENST00000430710.7:c.3660T>C	ENSP00000406288.3:p.Asn1220=
ENST00000555935.1:c.2173T>C
ENST00000555962.5:n.525-179T>C
ENST00000557364.5:c.4497T>C	ENSP00000451601.1:p.Asn1499=
NM_001170629.1:c.4497T>C	NP_001164100.1:p.Asn1499=
NM_020920.3:c.3660T>C	NP_065971.2:p.Asn1220=
NM_001170629.2:c.4497T>C MANE Select	NP_001164100.1:p.Asn1499=
NM_020920.4:c.3660T>C	NP_065971.2:p.Asn1220=