Canonical Allele Identifier: CA2122483062
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21409774_21409775delinsCA , CM000676.2:g.21409774_21409775delinsCA GRCh38
NC_000014.8:g.21877933_21877934delinsCA , CM000676.1:g.21877933_21877934delinsCA GRCh37
NC_000014.7:g.20947773_20947774delinsCA NCBI36
NG_021249.1:g.32524_32525delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.1527+76_1527+77delinsTG ENSP00000406288.3:n.1527+76_1527+77delins...
ENST00000555935.2:c.40+76_40+77delinsTG
ENST00000555962.6:c.-110-6733_-110-6732delinsTG ENSP00000495174.1:n.-110-6733_-110-6732de...
ENST00000557364.6:c.2364+76_2364+77delinsTG ENSP00000451601.1:n.2364+76_2364+77delins...
ENST00000643469.1:c.2364+76_2364+77delinsTG ENSP00000495070.1:n.2364+76_2364+77delins...
ENST00000645140.1:c.2276+76_2276+77delinsTG
ENST00000645206.1:n.878+76_878+77delinsTG
ENST00000645929.1:c.1527+76_1527+77delinsTG ENSP00000494402.1:n.1527+76_1527+77delins...
ENST00000646340.1:c.2370+76_2370+77delinsTG ENSP00000496730.1:n.2370+76_2370+77delins...
ENST00000646647.2:c.2364+76_2364+77delinsTG MANE Select ENSP00000495240.1:n.2364+76_2364+77delins...
ENST00000399982.6:c.2364+76_2364+77delinsTG ENSP00000382863.2:n.2364+76_2364+77delins...
ENST00000430710.7:c.1527+76_1527+77delinsTG ENSP00000406288.3:n.1527+76_1527+77delins...
ENST00000554384.1:n.232+76_232+77delinsTG
ENST00000555935.1:c.40+76_40+77delinsTG
ENST00000555962.5:n.151-6733_151-6732delinsTG
ENST00000557364.5:c.2364+76_2364+77delinsTG ENSP00000451601.1:n.2364+76_2364+77delins...
NM_001170629.1:c.2364+76_2364+77delinsTG NP_001164100.1:n.2364+76_2364+77delinsTG
NM_020920.3:c.1527+76_1527+77delinsTG NP_065971.2:n.1527+76_1527+77delinsTG
NM_001170629.2:c.2364+76_2364+77delinsTG MANE Select NP_001164100.1:n.2364+76_2364+77delinsTG
NM_020920.4:c.1527+76_1527+77delinsTG NP_065971.2:n.1527+76_1527+77delinsTG