Canonical Allele Identifier: CA1151337144
Gene: CHD5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6112194C= , CM000663.2:g.6112194C= GRCh38
NC_000001.10:g.6172254C= , CM000663.1:g.6172254C= GRCh37
NC_000001.9:g.6094841C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262450.8:c.5086G= MANE Select ENSP00000262450.3:p.Asp1696=
ENST00000262450.7:c.5086G= ENSP00000262450.3:p.Asp1696=
ENST00000377999.5:c.1989G= ENSP00000367238.2:n.1989G=
ENST00000462991.5:c.3339G=
ENST00000496404.1:c.3804G= ENSP00000433676.1:n.3804G=
NM_015557.2:c.5086G= NP_056372.1:p.Asp1696=
NM_015557.3:c.5086G= MANE Select NP_056372.1:p.Asp1696=
Search 100 bp 5'
Search 100 bp 3'