Canonical Allele Identifier: CA1587282464

Gene: HDAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626065A= , CM000667.2:g.141626065A=	GRCh38
NC_000005.9:g.141005632A= , CM000667.1:g.141005632A=	GRCh37
NC_000005.8:g.140985816A=	NCBI36
NG_029678.1:g.15792T=
NG_029678.2:g.15792T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.927T= MANE Select	ENSP00000302967.3:p.Tyr309=
ENST00000305264.7:c.927T=	ENSP00000302967.3:p.Tyr309=
ENST00000459727.5:n.233+129T=
ENST00000467533.5:n.599+129T=
ENST00000469207.5:n.6T=
ENST00000469550.6:n.1000T=
ENST00000475549.1:n.258T=
ENST00000486618.1:n.421T=
ENST00000491581.5:n.141T=
ENST00000492407.1:n.767+129T=
NM_003883.3:c.927T=	NP_003874.2:p.Tyr309=
XM_011537697.1:c.366T=	XP_011535999.1:p.Tyr122=
XR_944336.1:n.1012T=
NM_001355039.1:c.927T=	NP_001341968.1:p.Tyr309=
NM_001355040.1:c.468T=	NP_001341969.1:p.Tyr156=
NM_001355041.1:c.366T=	NP_001341970.1:p.Tyr122=
NR_149164.1:n.993T=
NR_149165.1:n.875T=
NR_149166.1:n.843+129T=
NR_149167.1:n.1011+129T=
NR_149168.1:n.1018T=
NR_149169.1:n.1018T=
NM_003883.4:c.927T= MANE Select	NP_003874.2:p.Tyr309=
NM_001355039.2:c.927T=	NP_001341968.1:p.Tyr309=
NR_149167.2:n.1004+129T=
NM_001355040.2:c.468T=	NP_001341969.1:p.Tyr156=
NM_001355041.2:c.366T=	NP_001341970.1:p.Tyr122=
NR_149164.2:n.986T=
NR_149165.2:n.868T=
NR_149166.2:n.836+129T=
NR_149168.2:n.1011T=
NR_149169.2:n.1011T=