Canonical Allele Identifier: CA2624084934

Gene: CHD8

Linked Data

• gnomAD v4: 14-21415421-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415421G>A , CM000676.2:g.21415421G>A	GRCh38
NC_000014.8:g.21883580G>A , CM000676.1:g.21883580G>A	GRCh37
NC_000014.7:g.20953420G>A	NCBI36
NG_021249.1:g.26878C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1131+153C>T	ENSP00000406288.3:n.1131+153C>T
ENST00000555962.6:c.-110-12379C>T	ENSP00000495174.1:n.-110-12379C>T
ENST00000557364.6:c.1968+153C>T	ENSP00000451601.1:n.1968+153C>T
ENST00000642914.1:n.1104C>T
ENST00000643469.1:c.1968+153C>T	ENSP00000495070.1:n.1968+153C>T
ENST00000645140.1:c.1880+153C>T
ENST00000645206.1:n.482+153C>T
ENST00000645929.1:c.1131+153C>T	ENSP00000494402.1:n.1131+153C>T
ENST00000646340.1:c.1974+153C>T	ENSP00000496730.1:n.1974+153C>T
ENST00000646647.2:c.1968+153C>T MANE Select	ENSP00000495240.1:n.1968+153C>T
ENST00000399982.6:c.1968+153C>T	ENSP00000382863.2:n.1968+153C>T
ENST00000430710.7:c.1131+153C>T	ENSP00000406288.3:n.1131+153C>T
ENST00000555962.5:n.151-12379C>T
ENST00000557364.5:c.1968+153C>T	ENSP00000451601.1:n.1968+153C>T
NM_001170629.1:c.1968+153C>T	NP_001164100.1:n.1968+153C>T
NM_020920.3:c.1131+153C>T	NP_065971.2:n.1131+153C>T
NM_001170629.2:c.1968+153C>T MANE Select	NP_001164100.1:n.1968+153C>T
NM_020920.4:c.1131+153C>T	NP_065971.2:n.1131+153C>T