Canonical Allele Identifier: CA1587292599

Gene: HDAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141634927T= , CM000667.2:g.141634927T=	GRCh38
NC_000005.9:g.141014494T= , CM000667.1:g.141014494T=	GRCh37
NC_000005.8:g.140994678T=	NCBI36
NG_029678.1:g.6930A=
NG_029678.2:g.6930A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.165A= MANE Select	ENSP00000302967.3:p.Gln55=
ENST00000305264.7:c.165A=	ENSP00000302967.3:p.Gln55=
ENST00000469550.6:n.238A=
ENST00000495485.1:n.200A=
ENST00000519474.5:c.138+1621A=	ENSP00000430782.1:n.138+1621A=
ENST00000523088.5:c.138+1621A=	ENSP00000429099.1:n.138+1621A=
NM_003883.3:c.165A=	NP_003874.2:p.Gln55=
XM_011537697.1:c.-281+1621A=	XP_011535999.1:n.-281+1621A=
XR_944336.1:n.225A=
NM_001355039.1:c.165A=	NP_001341968.1:p.Gln55=
NM_001355040.1:c.-123+1621A=	NP_001341969.1:n.-123+1621A=
NM_001355041.1:c.-281+1621A=	NP_001341970.1:n.-281+1621A=
NR_149164.1:n.231A=
NR_149165.1:n.204+1621A=
NR_149166.1:n.204+1621A=
NR_149167.1:n.231A=
NR_149168.1:n.231A=
NR_149169.1:n.231A=
NM_003883.4:c.165A= MANE Select	NP_003874.2:p.Gln55=
NM_001355039.2:c.165A=	NP_001341968.1:p.Gln55=
NR_149167.2:n.224A=
NM_001355040.2:c.-123+1621A=	NP_001341969.1:n.-123+1621A=
NM_001355041.2:c.-281+1621A=	NP_001341970.1:n.-281+1621A=
NR_149164.2:n.224A=
NR_149165.2:n.197+1621A=
NR_149166.2:n.197+1621A=
NR_149168.2:n.224A=
NR_149169.2:n.224A=