Canonical Allele Identifier: CA388885317

Gene: CHD8

Linked Data

• gnomAD v4: 14-21429211-G-T
• MyVariant Identifiers: chr14:g.21897370G>T (hg19) ; chr14:g.21429211G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429211G>T , CM000676.2:g.21429211G>T	GRCh38
NC_000014.8:g.21897370G>T , CM000676.1:g.21897370G>T	GRCh37
NC_000014.7:g.20967210G>T	NCBI36
NG_021249.1:g.13088C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.131C>A	ENSP00000406288.3:p.Ala44Asp
ENST00000553651.2:n.2774C>A
ENST00000555962.6:c.-111+2600C>A	ENSP00000495174.1:n.-111+2600C>A
ENST00000557364.6:c.968C>A	ENSP00000451601.1:p.Ala323Asp
ENST00000642518.1:c.131C>A	ENSP00000496722.1:p.Ala44Asp
ENST00000643048.1:n.1263C>A
ENST00000643469.1:c.968C>A	ENSP00000495070.1:p.Ala323Asp
ENST00000645140.1:c.880C>A
ENST00000645929.1:c.131C>A	ENSP00000494402.1:p.Ala44Asp
ENST00000646063.1:c.1055C>A	ENSP00000496565.1:p.Ala352Asp
ENST00000646340.1:c.974C>A	ENSP00000496730.1:p.Ala325Asp
ENST00000646647.2:c.968C>A MANE Select	ENSP00000495240.1:p.Ala323Asp
ENST00000399982.6:c.968C>A	ENSP00000382863.2:p.Ala323Asp
ENST00000430710.7:c.131C>A	ENSP00000406288.3:p.Ala44Asp
ENST00000553283.1:c.221C>A	ENSP00000450860.1:p.Ala74Asp
ENST00000555962.5:n.150+2600C>A
ENST00000557364.5:c.968C>A	ENSP00000451601.1:p.Ala323Asp
NM_001170629.1:c.968C>A	NP_001164100.1:p.Ala323Asp
NM_020920.3:c.131C>A	NP_065971.2:p.Ala44Asp
NM_001170629.2:c.968C>A MANE Select	NP_001164100.1:p.Ala323Asp
NM_020920.4:c.131C>A	NP_065971.2:p.Ala44Asp