Canonical Allele Identifier: CA2122506242
Gene: CHD8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21429314G= , CM000676.2:g.21429314G= GRCh38
NC_000014.8:g.21897473G= , CM000676.1:g.21897473G= GRCh37
NC_000014.7:g.20967313G= NCBI36
NG_021249.1:g.12985C=

Transcript Alleles

HGVS Amino-acid change
ENST00000430710.8:c.28C= ENSP00000406288.3:p.Leu10=
ENST00000553651.2:n.2671C=
ENST00000555962.6:c.-111+2497C= ENSP00000495174.1:n.-111+2497C=
ENST00000557364.6:c.865C= ENSP00000451601.1:p.Leu289=
ENST00000642518.1:c.28C= ENSP00000496722.1:p.Leu10=
ENST00000643048.1:n.1160C=
ENST00000643469.1:c.865C= ENSP00000495070.1:p.Leu289=
ENST00000645140.1:c.777C=
ENST00000645929.1:c.28C= ENSP00000494402.1:p.Leu10=
ENST00000646063.1:c.952C= ENSP00000496565.1:p.Leu318=
ENST00000646340.1:c.871C= ENSP00000496730.1:p.Leu291=
ENST00000646647.2:c.865C= MANE Select ENSP00000495240.1:p.Leu289=
ENST00000399982.6:c.865C= ENSP00000382863.2:p.Leu289=
ENST00000430710.7:c.28C= ENSP00000406288.3:p.Leu10=
ENST00000553283.1:c.118C= ENSP00000450860.1:p.Leu40=
ENST00000555962.5:n.150+2497C=
ENST00000557364.5:c.865C= ENSP00000451601.1:p.Leu289=
NM_001170629.1:c.865C= NP_001164100.1:p.Leu289=
NM_020920.3:c.28C= NP_065971.2:p.Leu10=
NM_001170629.2:c.865C= MANE Select NP_001164100.1:p.Leu289=
NM_020920.4:c.28C= NP_065971.2:p.Leu10=