Canonical Allele Identifier: CA388885101

Gene: CHD8

Linked Data

• MyVariant Identifiers: chr14:g.21897325A>G (hg19) ; chr14:g.21429166A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21429166A>G , CM000676.2:g.21429166A>G	GRCh38
NC_000014.8:g.21897325A>G , CM000676.1:g.21897325A>G	GRCh37
NC_000014.7:g.20967165A>G	NCBI36
NG_021249.1:g.13133T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430710.8:c.176T>C	ENSP00000406288.3:p.Val59Ala
ENST00000553651.2:n.2819T>C
ENST00000555962.6:c.-111+2645T>C	ENSP00000495174.1:n.-111+2645T>C
ENST00000557364.6:c.1013T>C	ENSP00000451601.1:p.Val338Ala
ENST00000642518.1:c.176T>C	ENSP00000496722.1:p.Val59Ala
ENST00000643048.1:n.1308T>C
ENST00000643469.1:c.1013T>C	ENSP00000495070.1:p.Val338Ala
ENST00000645140.1:c.925T>C
ENST00000645929.1:c.176T>C	ENSP00000494402.1:p.Val59Ala
ENST00000646063.1:c.1100T>C	ENSP00000496565.1:p.Val367Ala
ENST00000646340.1:c.1019T>C	ENSP00000496730.1:p.Val340Ala
ENST00000646647.2:c.1013T>C MANE Select	ENSP00000495240.1:p.Val338Ala
ENST00000399982.6:c.1013T>C	ENSP00000382863.2:p.Val338Ala
ENST00000430710.7:c.176T>C	ENSP00000406288.3:p.Val59Ala
ENST00000553283.1:c.266T>C	ENSP00000450860.1:p.Val89Ala
ENST00000555962.5:n.150+2645T>C
ENST00000557364.5:c.1013T>C	ENSP00000451601.1:p.Val338Ala
NM_001170629.1:c.1013T>C	NP_001164100.1:p.Val338Ala
NM_020920.3:c.176T>C	NP_065971.2:p.Val59Ala
NM_001170629.2:c.1013T>C MANE Select	NP_001164100.1:p.Val338Ala
NM_020920.4:c.176T>C	NP_065971.2:p.Val59Ala