Canonical Allele Identifier: CA1587282480

Gene: HDAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626124A= , CM000667.2:g.141626124A=	GRCh38
NC_000005.9:g.141005691A= , CM000667.1:g.141005691A=	GRCh37
NC_000005.8:g.140985875A=	NCBI36
NG_029678.1:g.15733T=
NG_029678.2:g.15733T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.921-53T= MANE Select	ENSP00000302967.3:n.921-53T=
ENST00000305264.7:c.921-53T=	ENSP00000302967.3:n.921-53T=
ENST00000459727.5:n.233+70T=
ENST00000467533.5:n.599+70T=
ENST00000469550.6:n.994-53T=
ENST00000475549.1:n.252-53T=
ENST00000486618.1:n.362T=
ENST00000491581.5:n.135-53T=
ENST00000492407.1:n.767+70T=
NM_003883.3:c.921-53T=	NP_003874.2:n.921-53T=
XM_011537697.1:c.360-53T=	XP_011535999.1:n.360-53T=
XR_944336.1:n.1006-53T=
NM_001355039.1:c.921-53T=	NP_001341968.1:n.921-53T=
NM_001355040.1:c.462-53T=	NP_001341969.1:n.462-53T=
NM_001355041.1:c.360-53T=	NP_001341970.1:n.360-53T=
NR_149164.1:n.987-53T=
NR_149165.1:n.869-53T=
NR_149166.1:n.843+70T=
NR_149167.1:n.1011+70T=
NR_149168.1:n.1012-53T=
NR_149169.1:n.1012-53T=
NM_003883.4:c.921-53T= MANE Select	NP_003874.2:n.921-53T=
NM_001355039.2:c.921-53T=	NP_001341968.1:n.921-53T=
NR_149167.2:n.1004+70T=
NM_001355040.2:c.462-53T=	NP_001341969.1:n.462-53T=
NM_001355041.2:c.360-53T=	NP_001341970.1:n.360-53T=
NR_149164.2:n.980-53T=
NR_149165.2:n.862-53T=
NR_149166.2:n.836+70T=
NR_149168.2:n.1005-53T=
NR_149169.2:n.1005-53T=