Canonical Allele Identifier: CA1587282452
Gene: HDAC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141626033C= , CM000667.2:g.141626033C= GRCh38
NC_000005.9:g.141005600C= , CM000667.1:g.141005600C= GRCh37
NC_000005.8:g.140985784C= NCBI36
NG_029678.1:g.15824G=
NG_029678.2:g.15824G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.959G= MANE Select ENSP00000302967.3:p.Ser320=
ENST00000305264.7:c.959G= ENSP00000302967.3:p.Ser320=
ENST00000459727.5:n.233+161G=
ENST00000467533.5:n.599+161G=
ENST00000469207.5:n.38G=
ENST00000469550.6:n.1032G=
ENST00000475549.1:n.290G=
ENST00000486618.1:n.453G=
ENST00000491581.5:n.173G=
ENST00000492407.1:n.767+161G=
NM_003883.3:c.959G= NP_003874.2:p.Ser320=
XM_011537697.1:c.398G= XP_011535999.1:p.Ser133=
XR_944336.1:n.1044G=
NM_001355039.1:c.959G= NP_001341968.1:p.Ser320=
NM_001355040.1:c.500G= NP_001341969.1:p.Ser167=
NM_001355041.1:c.398G= NP_001341970.1:p.Ser133=
NR_149164.1:n.1025G=
NR_149165.1:n.907G=
NR_149166.1:n.843+161G=
NR_149167.1:n.1011+161G=
NR_149168.1:n.1050G=
NR_149169.1:n.1050G=
NM_003883.4:c.959G= MANE Select NP_003874.2:p.Ser320=
NM_001355039.2:c.959G= NP_001341968.1:p.Ser320=
NR_149167.2:n.1004+161G=
NM_001355040.2:c.500G= NP_001341969.1:p.Ser167=
NM_001355041.2:c.398G= NP_001341970.1:p.Ser133=
NR_149164.2:n.1018G=
NR_149165.2:n.900G=
NR_149166.2:n.836+161G=
NR_149168.2:n.1043G=
NR_149169.2:n.1043G=