Canonical Allele Identifier: CA446894580

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005629C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626062C>T , CM000667.2:g.141626062C>T	GRCh38
NC_000005.9:g.141005629C>T , CM000667.1:g.141005629C>T	GRCh37
NC_000005.8:g.140985813C>T	NCBI36
NG_029678.1:g.15795G>A
NG_029678.2:g.15795G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.930G>A MANE Select	ENSP00000302967.3:p.Glu310=
ENST00000305264.7:c.930G>A	ENSP00000302967.3:p.Glu310=
ENST00000459727.5:n.233+132G>A
ENST00000467533.5:n.599+132G>A
ENST00000469207.5:n.9G>A
ENST00000469550.6:n.1003G>A
ENST00000475549.1:n.261G>A
ENST00000486618.1:n.424G>A
ENST00000491581.5:n.144G>A
ENST00000492407.1:n.767+132G>A
NM_003883.3:c.930G>A	NP_003874.2:p.Glu310=
XM_011537697.1:c.369G>A	XP_011535999.1:p.Glu123=
XR_944336.1:n.1015G>A
NM_001355039.1:c.930G>A	NP_001341968.1:p.Glu310=
NM_001355040.1:c.471G>A	NP_001341969.1:p.Glu157=
NM_001355041.1:c.369G>A	NP_001341970.1:p.Glu123=
NR_149164.1:n.996G>A
NR_149165.1:n.878G>A
NR_149166.1:n.843+132G>A
NR_149167.1:n.1011+132G>A
NR_149168.1:n.1021G>A
NR_149169.1:n.1021G>A
NM_003883.4:c.930G>A MANE Select	NP_003874.2:p.Glu310=
NM_001355039.2:c.930G>A	NP_001341968.1:p.Glu310=
NR_149167.2:n.1004+132G>A
NM_001355040.2:c.471G>A	NP_001341969.1:p.Glu157=
NM_001355041.2:c.369G>A	NP_001341970.1:p.Glu123=
NR_149164.2:n.989G>A
NR_149165.2:n.871G>A
NR_149166.2:n.836+132G>A
NR_149168.2:n.1014G>A
NR_149169.2:n.1014G>A