Canonical Allele Identifier: CA1151337184
Gene: CHD5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6112285G= , CM000663.2:g.6112285G= GRCh38
NC_000001.10:g.6172345G= , CM000663.1:g.6172345G= GRCh37
NC_000001.9:g.6094932G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262450.8:c.5003-8C= MANE Select ENSP00000262450.3:n.5003-8C=
ENST00000262450.7:c.5003-8C= ENSP00000262450.3:n.5003-8C=
ENST00000377999.5:c.1906-8C= ENSP00000367238.2:n.1906-8C=
ENST00000462991.5:c.3256-8C=
ENST00000496404.1:c.3721-8C= ENSP00000433676.1:n.3721-8C=
NM_015557.2:c.5003-8C= NP_056372.1:n.5003-8C=
NM_015557.3:c.5003-8C= MANE Select NP_056372.1:n.5003-8C=
Search 100 bp 5'
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