Canonical Allele Identifier: CA361515087
Gene: HDAC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141626027T>G , CM000667.2:g.141626027T>G GRCh38
NC_000005.9:g.141005594T>G , CM000667.1:g.141005594T>G GRCh37
NC_000005.8:g.140985778T>G NCBI36
NG_029678.1:g.15830A>C
NG_029678.2:g.15830A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.965A>C MANE Select ENSP00000302967.3:p.Glu322Ala
ENST00000305264.7:c.965A>C ENSP00000302967.3:p.Glu322Ala
ENST00000459727.5:n.233+167A>C
ENST00000467533.5:n.599+167A>C
ENST00000469207.5:n.44A>C
ENST00000469550.6:n.1038A>C
ENST00000475549.1:n.296A>C
ENST00000486618.1:n.459A>C
ENST00000491581.5:n.179A>C
ENST00000492407.1:n.767+167A>C
NM_003883.3:c.965A>C NP_003874.2:p.Glu322Ala
XM_011537697.1:c.404A>C XP_011535999.1:p.Glu135Ala
XR_944336.1:n.1050A>C
NM_001355039.1:c.965A>C NP_001341968.1:p.Glu322Ala
NM_001355040.1:c.506A>C NP_001341969.1:p.Glu169Ala
NM_001355041.1:c.404A>C NP_001341970.1:p.Glu135Ala
NR_149164.1:n.1031A>C
NR_149165.1:n.913A>C
NR_149166.1:n.843+167A>C
NR_149167.1:n.1011+167A>C
NR_149168.1:n.1056A>C
NR_149169.1:n.1056A>C
NM_003883.4:c.965A>C MANE Select NP_003874.2:p.Glu322Ala
NM_001355039.2:c.965A>C NP_001341968.1:p.Glu322Ala
NR_149167.2:n.1004+167A>C
NM_001355040.2:c.506A>C NP_001341969.1:p.Glu169Ala
NM_001355041.2:c.404A>C NP_001341970.1:p.Glu135Ala
NR_149164.2:n.1024A>C
NR_149165.2:n.906A>C
NR_149166.2:n.836+167A>C
NR_149168.2:n.1049A>C
NR_149169.2:n.1049A>C