Canonical Allele Identifier: CA2624085070
Gene: CHD8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21415551_21415558del , CM000676.2:g.21415551_21415558del GRCh38
NC_000014.8:g.21883710_21883717del , CM000676.1:g.21883710_21883717del GRCh37
NC_000014.7:g.20953550_20953557del NCBI36
NG_021249.1:g.26742_26749del

Transcript Alleles

HGVS Amino-acid Change
ENST00000430710.8:c.1131+17_1131+24del ENSP00000406288.3:n.1131+17_1131+24del
ENST00000555962.6:c.-110-12515_-110-12508del ENSP00000495174.1:n.-110-12515_-110-12508del
ENST00000557364.6:c.1968+17_1968+24del ENSP00000451601.1:n.1968+17_1968+24del
ENST00000642914.1:n.968_975del
ENST00000643469.1:c.1968+17_1968+24del ENSP00000495070.1:n.1968+17_1968+24del
ENST00000645140.1:c.1880+17_1880+24del
ENST00000645206.1:n.482+17_482+24del
ENST00000645929.1:c.1131+17_1131+24del ENSP00000494402.1:n.1131+17_1131+24del
ENST00000646340.1:c.1974+17_1974+24del ENSP00000496730.1:n.1974+17_1974+24del
ENST00000646647.2:c.1968+17_1968+24del MANE Select ENSP00000495240.1:n.1968+17_1968+24del
ENST00000399982.6:c.1968+17_1968+24del ENSP00000382863.2:n.1968+17_1968+24del
ENST00000430710.7:c.1131+17_1131+24del ENSP00000406288.3:n.1131+17_1131+24del
ENST00000555962.5:n.151-12515_151-12508del
ENST00000557364.5:c.1968+17_1968+24del ENSP00000451601.1:n.1968+17_1968+24del
NM_001170629.1:c.1968+17_1968+24del NP_001164100.1:n.1968+17_1968+24del
NM_020920.3:c.1131+17_1131+24del NP_065971.2:n.1131+17_1131+24del
NM_001170629.2:c.1968+17_1968+24del MANE Select NP_001164100.1:n.1968+17_1968+24del
NM_020920.4:c.1131+17_1131+24del NP_065971.2:n.1131+17_1131+24del