Canonical Allele Identifier: CA1587281988

Gene: HDAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624821A= , CM000667.2:g.141624821A=	GRCh38
NC_000005.9:g.141004388A= , CM000667.1:g.141004388A=	GRCh37
NC_000005.8:g.140984572A=	NCBI36
NG_029678.1:g.17036T=
NG_029678.2:g.17036T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.1217+387T= MANE Select	ENSP00000302967.3:n.1217+387T=
ENST00000305264.7:c.1217+387T=	ENSP00000302967.3:n.1217+387T=
ENST00000459727.5:n.471+387T=
ENST00000469207.5:n.216+387T=
ENST00000469550.6:n.1290+387T=
NM_003883.3:c.1217+387T=	NP_003874.2:n.1217+387T=
XM_011537697.1:c.656+387T=	XP_011535999.1:n.656+387T=
XR_427789.2:n.231-1026A=
XR_944336.1:n.1302+387T=
NM_001355040.1:c.758+387T=	NP_001341969.1:n.758+387T=
NM_001355041.1:c.656+387T=	NP_001341970.1:n.656+387T=
NR_149164.1:n.1203+387T=
NR_149165.1:n.1165+387T=
NR_149166.1:n.1081+387T=
NR_149168.1:n.1308+387T=
NR_149169.1:n.1228+387T=
NM_003883.4:c.1217+387T= MANE Select	NP_003874.2:n.1217+387T=
NM_001355040.2:c.758+387T=	NP_001341969.1:n.758+387T=
NM_001355041.2:c.656+387T=	NP_001341970.1:n.656+387T=
NR_149164.2:n.1196+387T=
NR_149165.2:n.1158+387T=
NR_149166.2:n.1074+387T=
NR_149168.2:n.1301+387T=
NR_149169.2:n.1221+387T=