Canonical Allele Identifier: CA1147663639

Gene: CHD5

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.6112283G= , CM000663.2:g.6112283G=	GRCh38
NC_000001.10:g.6172343G= , CM000663.1:g.6172343G=	GRCh37
NC_000001.9:g.6094930G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262450.8:c.5003-6C= MANE Select	ENSP00000262450.3:n.5003-6C=
ENST00000262450.7:c.5003-6C=	ENSP00000262450.3:n.5003-6C=
ENST00000377999.5:c.1906-6C=	ENSP00000367238.2:n.1906-6C=
ENST00000462991.5:c.3256-6C=
ENST00000496404.1:c.3721-6C=	ENSP00000433676.1:n.3721-6C=
NM_015557.2:c.5003-6C=	NP_056372.1:n.5003-6C=
NM_015557.3:c.5003-6C= MANE Select	NP_056372.1:n.5003-6C=