Canonical Allele Identifier: CA2122502128

Gene: CHD8

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21405605_21405606delinsCA , CM000676.2:g.21405605_21405606delinsCA	GRCh38
NC_000014.8:g.21873764_21873765delinsCA , CM000676.1:g.21873764_21873765delinsCA	GRCh37
NC_000014.7:g.20943604_20943605delinsCA	NCBI36
NG_021249.1:g.36693_36694delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.2214+115_2214+116delinsTG	ENSP00000406288.3:n.2214+115_2214+116delinsTG
ENST00000555935.2:c.727+115_727+116delinsTG
ENST00000555962.6:c.-110-2564_-110-2563delinsTG	ENSP00000495174.1:n.-110-2564_-110-2563delinsTG
ENST00000557364.6:c.3051+115_3051+116delinsTG	ENSP00000451601.1:n.3051+115_3051+116delinsTG
ENST00000643469.1:c.3051+115_3051+116delinsTG	ENSP00000495070.1:n.3051+115_3051+116delinsTG
ENST00000645140.1:c.2963+115_2963+116delinsTG
ENST00000645206.1:n.1565+115_1565+116delinsTG
ENST00000645929.1:c.2214+115_2214+116delinsTG	ENSP00000494402.1:n.2214+115_2214+116delinsTG
ENST00000646340.1:c.3057+115_3057+116delinsTG	ENSP00000496730.1:n.3057+115_3057+116delinsTG
ENST00000646647.2:c.3051+115_3051+116delinsTG MANE Select	ENSP00000495240.1:n.3051+115_3051+116delinsTG
ENST00000399982.6:c.3051+115_3051+116delinsTG	ENSP00000382863.2:n.3051+115_3051+116delinsTG
ENST00000430710.7:c.2214+115_2214+116delinsTG	ENSP00000406288.3:n.2214+115_2214+116delinsTG
ENST00000555935.1:c.727+115_727+116delinsTG
ENST00000555962.5:n.151-2564_151-2563delinsTG
ENST00000557364.5:c.3051+115_3051+116delinsTG	ENSP00000451601.1:n.3051+115_3051+116delinsTG
NM_001170629.1:c.3051+115_3051+116delinsTG	NP_001164100.1:n.3051+115_3051+116delinsTG
NM_020920.3:c.2214+115_2214+116delinsTG	NP_065971.2:n.2214+115_2214+116delinsTG
NM_001170629.2:c.3051+115_3051+116delinsTG MANE Select	NP_001164100.1:n.3051+115_3051+116delinsTG
NM_020920.4:c.2214+115_2214+116delinsTG	NP_065971.2:n.2214+115_2214+116delinsTG