Canonical Allele Identifier: CA1587281970

Gene: HDAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624764A= , CM000667.2:g.141624764A=	GRCh38
NC_000005.9:g.141004331A= , CM000667.1:g.141004331A=	GRCh37
NC_000005.8:g.140984515A=	NCBI36
NG_029678.1:g.17093T=
NG_029678.2:g.17093T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.1217+444T= MANE Select	ENSP00000302967.3:n.1217+444T=
ENST00000305264.7:c.1217+444T=	ENSP00000302967.3:n.1217+444T=
ENST00000459727.5:n.471+444T=
ENST00000469207.5:n.216+444T=
ENST00000469550.6:n.1290+444T=
NM_003883.3:c.1217+444T=	NP_003874.2:n.1217+444T=
XM_011537697.1:c.656+444T=	XP_011535999.1:n.656+444T=
XR_427789.2:n.231-1083A=
XR_944336.1:n.1302+444T=
NM_001355040.1:c.758+444T=	NP_001341969.1:n.758+444T=
NM_001355041.1:c.656+444T=	NP_001341970.1:n.656+444T=
NR_149164.1:n.1203+444T=
NR_149165.1:n.1165+444T=
NR_149166.1:n.1081+444T=
NR_149168.1:n.1308+444T=
NR_149169.1:n.1228+444T=
NM_003883.4:c.1217+444T= MANE Select	NP_003874.2:n.1217+444T=
NM_001355040.2:c.758+444T=	NP_001341969.1:n.758+444T=
NM_001355041.2:c.656+444T=	NP_001341970.1:n.656+444T=
NR_149164.2:n.1196+444T=
NR_149165.2:n.1158+444T=
NR_149166.2:n.1074+444T=
NR_149168.2:n.1301+444T=
NR_149169.2:n.1221+444T=