Canonical Allele Identifier: CA2624085069

Gene: CHD8

Linked Data

• gnomAD v4: 14-21415549-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21415551_21415552del , CM000676.2:g.21415551_21415552del	GRCh38
NC_000014.8:g.21883710_21883711del , CM000676.1:g.21883710_21883711del	GRCh37
NC_000014.7:g.20953550_20953551del	NCBI36
NG_021249.1:g.26748_26749del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.1131+23_1131+24del	ENSP00000406288.3:n.1131+23_1131+24del
ENST00000555962.6:c.-110-12509_-110-12508del	ENSP00000495174.1:n.-110-12509_-110-12508del
ENST00000557364.6:c.1968+23_1968+24del	ENSP00000451601.1:n.1968+23_1968+24del
ENST00000642914.1:n.974_975del
ENST00000643469.1:c.1968+23_1968+24del	ENSP00000495070.1:n.1968+23_1968+24del
ENST00000645140.1:c.1880+23_1880+24del
ENST00000645206.1:n.482+23_482+24del
ENST00000645929.1:c.1131+23_1131+24del	ENSP00000494402.1:n.1131+23_1131+24del
ENST00000646340.1:c.1974+23_1974+24del	ENSP00000496730.1:n.1974+23_1974+24del
ENST00000646647.2:c.1968+23_1968+24del MANE Select	ENSP00000495240.1:n.1968+23_1968+24del
ENST00000399982.6:c.1968+23_1968+24del	ENSP00000382863.2:n.1968+23_1968+24del
ENST00000430710.7:c.1131+23_1131+24del	ENSP00000406288.3:n.1131+23_1131+24del
ENST00000555962.5:n.151-12509_151-12508del
ENST00000557364.5:c.1968+23_1968+24del	ENSP00000451601.1:n.1968+23_1968+24del
NM_001170629.1:c.1968+23_1968+24del	NP_001164100.1:n.1968+23_1968+24del
NM_020920.3:c.1131+23_1131+24del	NP_065971.2:n.1131+23_1131+24del
NM_001170629.2:c.1968+23_1968+24del MANE Select	NP_001164100.1:n.1968+23_1968+24del
NM_020920.4:c.1131+23_1131+24del	NP_065971.2:n.1131+23_1131+24del