Canonical Allele Identifier: CA446894565

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005626T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626059T>A , CM000667.2:g.141626059T>A	GRCh38
NC_000005.9:g.141005626T>A , CM000667.1:g.141005626T>A	GRCh37
NC_000005.8:g.140985810T>A	NCBI36
NG_029678.1:g.15798A>T
NG_029678.2:g.15798A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.933A>T MANE Select	ENSP00000302967.3:p.Thr311=
ENST00000305264.7:c.933A>T	ENSP00000302967.3:p.Thr311=
ENST00000459727.5:n.233+135A>T
ENST00000467533.5:n.599+135A>T
ENST00000469207.5:n.12A>T
ENST00000469550.6:n.1006A>T
ENST00000475549.1:n.264A>T
ENST00000486618.1:n.427A>T
ENST00000491581.5:n.147A>T
ENST00000492407.1:n.767+135A>T
NM_003883.3:c.933A>T	NP_003874.2:p.Thr311=
XM_011537697.1:c.372A>T	XP_011535999.1:p.Thr124=
XR_944336.1:n.1018A>T
NM_001355039.1:c.933A>T	NP_001341968.1:p.Thr311=
NM_001355040.1:c.474A>T	NP_001341969.1:p.Thr158=
NM_001355041.1:c.372A>T	NP_001341970.1:p.Thr124=
NR_149164.1:n.999A>T
NR_149165.1:n.881A>T
NR_149166.1:n.843+135A>T
NR_149167.1:n.1011+135A>T
NR_149168.1:n.1024A>T
NR_149169.1:n.1024A>T
NM_003883.4:c.933A>T MANE Select	NP_003874.2:p.Thr311=
NM_001355039.2:c.933A>T	NP_001341968.1:p.Thr311=
NR_149167.2:n.1004+135A>T
NM_001355040.2:c.474A>T	NP_001341969.1:p.Thr158=
NM_001355041.2:c.372A>T	NP_001341970.1:p.Thr124=
NR_149164.2:n.992A>T
NR_149165.2:n.874A>T
NR_149166.2:n.836+135A>T
NR_149168.2:n.1017A>T
NR_149169.2:n.1017A>T