Canonical Allele Identifier: CA1144036689

Gene: CHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6112174C= , CM000663.2:g.6112174C=	GRCh38
NC_000001.10:g.6172234C= , CM000663.1:g.6172234C=	GRCh37
NC_000001.9:g.6094821C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262450.8:c.5106G= MANE Select	ENSP00000262450.3:p.Lys1702=
ENST00000262450.7:c.5106G=	ENSP00000262450.3:p.Lys1702=
ENST00000377999.5:c.2009G=	ENSP00000367238.2:n.2009G=
ENST00000462991.5:c.3359G=
ENST00000496404.1:c.3824G=	ENSP00000433676.1:n.3824G=
NM_015557.2:c.5106G=	NP_056372.1:p.Lys1702=
NM_015557.3:c.5106G= MANE Select	NP_056372.1:p.Lys1702=