Canonical Allele Identifier: CA1587282449

Gene: HDAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626021G= , CM000667.2:g.141626021G=	GRCh38
NC_000005.9:g.141005588G= , CM000667.1:g.141005588G=	GRCh37
NC_000005.8:g.140985772G=	NCBI36
NG_029678.1:g.15836C=
NG_029678.2:g.15836C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.971C= MANE Select	ENSP00000302967.3:p.Pro324=
ENST00000305264.7:c.971C=	ENSP00000302967.3:p.Pro324=
ENST00000459727.5:n.233+173C=
ENST00000467533.5:n.599+173C=
ENST00000469207.5:n.50C=
ENST00000469550.6:n.1044C=
ENST00000486618.1:n.465C=
ENST00000491581.5:n.185C=
ENST00000492407.1:n.767+173C=
NM_003883.3:c.971C=	NP_003874.2:p.Pro324=
XM_011537697.1:c.410C=	XP_011535999.1:p.Pro137=
XR_944336.1:n.1056C=
NM_001355039.1:c.971C=	NP_001341968.1:p.Pro324=
NM_001355040.1:c.512C=	NP_001341969.1:p.Pro171=
NM_001355041.1:c.410C=	NP_001341970.1:p.Pro137=
NR_149164.1:n.1037C=
NR_149165.1:n.919C=
NR_149166.1:n.843+173C=
NR_149167.1:n.1011+173C=
NR_149168.1:n.1062C=
NR_149169.1:n.1062C=
NM_003883.4:c.971C= MANE Select	NP_003874.2:p.Pro324=
NM_001355039.2:c.971C=	NP_001341968.1:p.Pro324=
NR_149167.2:n.1004+173C=
NM_001355040.2:c.512C=	NP_001341969.1:p.Pro171=
NM_001355041.2:c.410C=	NP_001341970.1:p.Pro137=
NR_149164.2:n.1030C=
NR_149165.2:n.912C=
NR_149166.2:n.836+173C=
NR_149168.2:n.1055C=
NR_149169.2:n.1055C=