Canonical Allele Identifier: CA361515479
Gene: HDAC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141626062C>A , CM000667.2:g.141626062C>A GRCh38
NC_000005.9:g.141005629C>A , CM000667.1:g.141005629C>A GRCh37
NC_000005.8:g.140985813C>A NCBI36
NG_029678.1:g.15795G>T
NG_029678.2:g.15795G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.930G>T MANE Select ENSP00000302967.3:p.Glu310Asp
ENST00000305264.7:c.930G>T ENSP00000302967.3:p.Glu310Asp
ENST00000459727.5:n.233+132G>T
ENST00000467533.5:n.599+132G>T
ENST00000469207.5:n.9G>T
ENST00000469550.6:n.1003G>T
ENST00000475549.1:n.261G>T
ENST00000486618.1:n.424G>T
ENST00000491581.5:n.144G>T
ENST00000492407.1:n.767+132G>T
NM_003883.3:c.930G>T NP_003874.2:p.Glu310Asp
XM_011537697.1:c.369G>T XP_011535999.1:p.Glu123Asp
XR_944336.1:n.1015G>T
NM_001355039.1:c.930G>T NP_001341968.1:p.Glu310Asp
NM_001355040.1:c.471G>T NP_001341969.1:p.Glu157Asp
NM_001355041.1:c.369G>T NP_001341970.1:p.Glu123Asp
NR_149164.1:n.996G>T
NR_149165.1:n.878G>T
NR_149166.1:n.843+132G>T
NR_149167.1:n.1011+132G>T
NR_149168.1:n.1021G>T
NR_149169.1:n.1021G>T
NM_003883.4:c.930G>T MANE Select NP_003874.2:p.Glu310Asp
NM_001355039.2:c.930G>T NP_001341968.1:p.Glu310Asp
NR_149167.2:n.1004+132G>T
NM_001355040.2:c.471G>T NP_001341969.1:p.Glu157Asp
NM_001355041.2:c.369G>T NP_001341970.1:p.Glu123Asp
NR_149164.2:n.989G>T
NR_149165.2:n.871G>T
NR_149166.2:n.836+132G>T
NR_149168.2:n.1014G>T
NR_149169.2:n.1014G>T