Canonical Allele Identifier: CA1587282451

Gene: HDAC3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.963G= MANE Select	ENSP00000302967.3:p.Glu321=
ENST00000305264.7:c.963G=	ENSP00000302967.3:p.Glu321=
ENST00000459727.5:n.233+165G=
ENST00000467533.5:n.599+165G=
ENST00000469207.5:n.42G=
ENST00000469550.6:n.1036G=
ENST00000475549.1:n.294G=
ENST00000486618.1:n.457G=
ENST00000491581.5:n.177G=
ENST00000492407.1:n.767+165G=
NM_003883.3:c.963G=	NP_003874.2:p.Glu321=
XM_011537697.1:c.402G=	XP_011535999.1:p.Glu134=
XR_944336.1:n.1048G=
NM_001355039.1:c.963G=	NP_001341968.1:p.Glu321=
NM_001355040.1:c.504G=	NP_001341969.1:p.Glu168=
NM_001355041.1:c.402G=	NP_001341970.1:p.Glu134=
NR_149164.1:n.1029G=
NR_149165.1:n.911G=
NR_149166.1:n.843+165G=
NR_149167.1:n.1011+165G=
NR_149168.1:n.1054G=
NR_149169.1:n.1054G=
NM_003883.4:c.963G= MANE Select	NP_003874.2:p.Glu321=
NM_001355039.2:c.963G=	NP_001341968.1:p.Glu321=
NR_149167.2:n.1004+165G=
NM_001355040.2:c.504G=	NP_001341969.1:p.Glu168=
NM_001355041.2:c.402G=	NP_001341970.1:p.Glu134=
NR_149164.2:n.1022G=
NR_149165.2:n.904G=
NR_149166.2:n.836+165G=
NR_149168.2:n.1047G=
NR_149169.2:n.1047G=