Canonical Allele Identifier: CA2624085053

Gene: CHD8

Linked Data

• gnomAD v4: 14-21406839-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21406839G>T , CM000676.2:g.21406839G>T	GRCh38
NC_000014.8:g.21874998G>T , CM000676.1:g.21874998G>T	GRCh37
NC_000014.7:g.20944838G>T	NCBI36
NG_021249.1:g.35460C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.2070+17C>A	ENSP00000406288.3:n.2070+17C>A
ENST00000555935.2:c.583+17C>A
ENST00000555962.6:c.-110-3797C>A	ENSP00000495174.1:n.-110-3797C>A
ENST00000557364.6:c.2907+17C>A	ENSP00000451601.1:n.2907+17C>A
ENST00000643469.1:c.2907+17C>A	ENSP00000495070.1:n.2907+17C>A
ENST00000645140.1:c.2819+17C>A
ENST00000645206.1:n.1421+17C>A
ENST00000645929.1:c.2070+17C>A	ENSP00000494402.1:n.2070+17C>A
ENST00000646340.1:c.2913+17C>A	ENSP00000496730.1:n.2913+17C>A
ENST00000646647.2:c.2907+17C>A MANE Select	ENSP00000495240.1:n.2907+17C>A
ENST00000399982.6:c.2907+17C>A	ENSP00000382863.2:n.2907+17C>A
ENST00000430710.7:c.2070+17C>A	ENSP00000406288.3:n.2070+17C>A
ENST00000555935.1:c.583+17C>A
ENST00000555962.5:n.151-3797C>A
ENST00000557364.5:c.2907+17C>A	ENSP00000451601.1:n.2907+17C>A
NM_001170629.1:c.2907+17C>A	NP_001164100.1:n.2907+17C>A
NM_020920.3:c.2070+17C>A	NP_065971.2:n.2070+17C>A
NM_001170629.2:c.2907+17C>A MANE Select	NP_001164100.1:n.2907+17C>A
NM_020920.4:c.2070+17C>A	NP_065971.2:n.2070+17C>A