Canonical Allele Identifier: CA446894458

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005602A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626035A>T , CM000667.2:g.141626035A>T	GRCh38
NC_000005.9:g.141005602A>T , CM000667.1:g.141005602A>T	GRCh37
NC_000005.8:g.140985786A>T	NCBI36
NG_029678.1:g.15822T>A
NG_029678.2:g.15822T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.957T>A MANE Select	ENSP00000302967.3:p.Ile319=
ENST00000305264.7:c.957T>A	ENSP00000302967.3:p.Ile319=
ENST00000459727.5:n.233+159T>A
ENST00000467533.5:n.599+159T>A
ENST00000469207.5:n.36T>A
ENST00000469550.6:n.1030T>A
ENST00000475549.1:n.288T>A
ENST00000486618.1:n.451T>A
ENST00000491581.5:n.171T>A
ENST00000492407.1:n.767+159T>A
NM_003883.3:c.957T>A	NP_003874.2:p.Ile319=
XM_011537697.1:c.396T>A	XP_011535999.1:p.Ile132=
XR_944336.1:n.1042T>A
NM_001355039.1:c.957T>A	NP_001341968.1:p.Ile319=
NM_001355040.1:c.498T>A	NP_001341969.1:p.Ile166=
NM_001355041.1:c.396T>A	NP_001341970.1:p.Ile132=
NR_149164.1:n.1023T>A
NR_149165.1:n.905T>A
NR_149166.1:n.843+159T>A
NR_149167.1:n.1011+159T>A
NR_149168.1:n.1048T>A
NR_149169.1:n.1048T>A
NM_003883.4:c.957T>A MANE Select	NP_003874.2:p.Ile319=
NM_001355039.2:c.957T>A	NP_001341968.1:p.Ile319=
NR_149167.2:n.1004+159T>A
NM_001355040.2:c.498T>A	NP_001341969.1:p.Ile166=
NM_001355041.2:c.396T>A	NP_001341970.1:p.Ile132=
NR_149164.2:n.1016T>A
NR_149165.2:n.898T>A
NR_149166.2:n.836+159T>A
NR_149168.2:n.1041T>A
NR_149169.2:n.1041T>A