Canonical Allele Identifier: CA1151361008
Gene: CHD5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.6144012C= , CM000663.2:g.6144012C= GRCh38
NC_000001.10:g.6204072C= , CM000663.1:g.6204072C= GRCh37
NC_000001.9:g.6126659C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262450.8:c.1934+12G= MANE Select ENSP00000262450.3:n.1934+12G=
ENST00000262450.7:c.1934+12G= ENSP00000262450.3:n.1934+12G=
ENST00000462991.5:c.81+12G=
ENST00000496404.1:c.1934+12G= ENSP00000433676.1:n.1934+12G=
NM_015557.2:c.1934+12G= NP_056372.1:n.1934+12G=
NM_015557.3:c.1934+12G= MANE Select NP_056372.1:n.1934+12G=
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