Canonical Allele Identifier: CA361515102
Gene: HDAC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141626029C>A , CM000667.2:g.141626029C>A GRCh38
NC_000005.9:g.141005596C>A , CM000667.1:g.141005596C>A GRCh37
NC_000005.8:g.140985780C>A NCBI36
NG_029678.1:g.15828G>T
NG_029678.2:g.15828G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.963G>T MANE Select ENSP00000302967.3:p.Glu321Asp
ENST00000305264.7:c.963G>T ENSP00000302967.3:p.Glu321Asp
ENST00000459727.5:n.233+165G>T
ENST00000467533.5:n.599+165G>T
ENST00000469207.5:n.42G>T
ENST00000469550.6:n.1036G>T
ENST00000475549.1:n.294G>T
ENST00000486618.1:n.457G>T
ENST00000491581.5:n.177G>T
ENST00000492407.1:n.767+165G>T
NM_003883.3:c.963G>T NP_003874.2:p.Glu321Asp
XM_011537697.1:c.402G>T XP_011535999.1:p.Glu134Asp
XR_944336.1:n.1048G>T
NM_001355039.1:c.963G>T NP_001341968.1:p.Glu321Asp
NM_001355040.1:c.504G>T NP_001341969.1:p.Glu168Asp
NM_001355041.1:c.402G>T NP_001341970.1:p.Glu134Asp
NR_149164.1:n.1029G>T
NR_149165.1:n.911G>T
NR_149166.1:n.843+165G>T
NR_149167.1:n.1011+165G>T
NR_149168.1:n.1054G>T
NR_149169.1:n.1054G>T
NM_003883.4:c.963G>T MANE Select NP_003874.2:p.Glu321Asp
NM_001355039.2:c.963G>T NP_001341968.1:p.Glu321Asp
NR_149167.2:n.1004+165G>T
NM_001355040.2:c.504G>T NP_001341969.1:p.Glu168Asp
NM_001355041.2:c.402G>T NP_001341970.1:p.Glu134Asp
NR_149164.2:n.1022G>T
NR_149165.2:n.904G>T
NR_149166.2:n.836+165G>T
NR_149168.2:n.1047G>T
NR_149169.2:n.1047G>T