Canonical Allele Identifier: CA1587281979

Gene: HDAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624794G= , CM000667.2:g.141624794G=	GRCh38
NC_000005.9:g.141004361G= , CM000667.1:g.141004361G=	GRCh37
NC_000005.8:g.140984545G=	NCBI36
NG_029678.1:g.17063C=
NG_029678.2:g.17063C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000305264.8:c.1217+414C= MANE Select	ENSP00000302967.3:n.1217+414C=
ENST00000305264.7:c.1217+414C=	ENSP00000302967.3:n.1217+414C=
ENST00000459727.5:n.471+414C=
ENST00000469207.5:n.216+414C=
ENST00000469550.6:n.1290+414C=
NM_003883.3:c.1217+414C=	NP_003874.2:n.1217+414C=
XM_011537697.1:c.656+414C=	XP_011535999.1:n.656+414C=
XR_427789.2:n.231-1053G=
XR_944336.1:n.1302+414C=
NM_001355040.1:c.758+414C=	NP_001341969.1:n.758+414C=
NM_001355041.1:c.656+414C=	NP_001341970.1:n.656+414C=
NR_149164.1:n.1203+414C=
NR_149165.1:n.1165+414C=
NR_149166.1:n.1081+414C=
NR_149168.1:n.1308+414C=
NR_149169.1:n.1228+414C=
NM_003883.4:c.1217+414C= MANE Select	NP_003874.2:n.1217+414C=
NM_001355040.2:c.758+414C=	NP_001341969.1:n.758+414C=
NM_001355041.2:c.656+414C=	NP_001341970.1:n.656+414C=
NR_149164.2:n.1196+414C=
NR_149165.2:n.1158+414C=
NR_149166.2:n.1074+414C=
NR_149168.2:n.1301+414C=
NR_149169.2:n.1221+414C=