Canonical Allele Identifier: CA1587282483

Gene: HDAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626127T= , CM000667.2:g.141626127T=	GRCh38
NC_000005.9:g.141005694T= , CM000667.1:g.141005694T=	GRCh37
NC_000005.8:g.140985878T=	NCBI36
NG_029678.1:g.15730A=
NG_029678.2:g.15730A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.921-56A= MANE Select	ENSP00000302967.3:n.921-56A=
ENST00000305264.7:c.921-56A=	ENSP00000302967.3:n.921-56A=
ENST00000459727.5:n.233+67A=
ENST00000467533.5:n.599+67A=
ENST00000469550.6:n.994-56A=
ENST00000475549.1:n.252-56A=
ENST00000486618.1:n.359A=
ENST00000491581.5:n.135-56A=
ENST00000492407.1:n.767+67A=
NM_003883.3:c.921-56A=	NP_003874.2:n.921-56A=
XM_011537697.1:c.360-56A=	XP_011535999.1:n.360-56A=
XR_944336.1:n.1006-56A=
NM_001355039.1:c.921-56A=	NP_001341968.1:n.921-56A=
NM_001355040.1:c.462-56A=	NP_001341969.1:n.462-56A=
NM_001355041.1:c.360-56A=	NP_001341970.1:n.360-56A=
NR_149164.1:n.987-56A=
NR_149165.1:n.869-56A=
NR_149166.1:n.843+67A=
NR_149167.1:n.1011+67A=
NR_149168.1:n.1012-56A=
NR_149169.1:n.1012-56A=
NM_003883.4:c.921-56A= MANE Select	NP_003874.2:n.921-56A=
NM_001355039.2:c.921-56A=	NP_001341968.1:n.921-56A=
NR_149167.2:n.1004+67A=
NM_001355040.2:c.462-56A=	NP_001341969.1:n.462-56A=
NM_001355041.2:c.360-56A=	NP_001341970.1:n.360-56A=
NR_149164.2:n.980-56A=
NR_149165.2:n.862-56A=
NR_149166.2:n.836+67A=
NR_149168.2:n.1005-56A=
NR_149169.2:n.1005-56A=