Canonical Allele Identifier: CA484987390

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21883953A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415794A>G , CM000676.2:g.21415794A>G	GRCh38
NC_000014.8:g.21883953A>G , CM000676.1:g.21883953A>G	GRCh37
NC_000014.7:g.20953793A>G	NCBI36
NG_021249.1:g.26505T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000430710.8:c.993T>C	ENSP00000406288.3:p.Pro331=
ENST00000555962.6:c.-110-12752T>C	ENSP00000495174.1:n.-110-12752T>C
ENST00000557364.6:c.1830T>C	ENSP00000451601.1:p.Pro610=
ENST00000642914.1:n.813T>C
ENST00000643469.1:c.1830T>C	ENSP00000495070.1:p.Pro610=
ENST00000645140.1:c.1742T>C
ENST00000645206.1:n.344T>C
ENST00000645929.1:c.993T>C	ENSP00000494402.1:p.Pro331=
ENST00000646340.1:c.1836T>C	ENSP00000496730.1:p.Pro612=
ENST00000646647.2:c.1830T>C MANE Select	ENSP00000495240.1:p.Pro610=
ENST00000399982.6:c.1830T>C	ENSP00000382863.2:p.Pro610=
ENST00000430710.7:c.993T>C	ENSP00000406288.3:p.Pro331=
ENST00000555962.5:n.151-12752T>C
ENST00000557364.5:c.1830T>C	ENSP00000451601.1:p.Pro610=
NM_001170629.1:c.1830T>C	NP_001164100.1:p.Pro610=
NM_020920.3:c.993T>C	NP_065971.2:p.Pro331=
NM_001170629.2:c.1830T>C MANE Select	NP_001164100.1:p.Pro610=
NM_020920.4:c.993T>C	NP_065971.2:p.Pro331=