Canonical Allele Identifier: CA361515459

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005627G>C (hg19) ; chr5:g.141626060G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626060G>C , CM000667.2:g.141626060G>C	GRCh38
NC_000005.9:g.141005627G>C , CM000667.1:g.141005627G>C	GRCh37
NC_000005.8:g.140985811G>C	NCBI36
NG_029678.1:g.15797C>G
NG_029678.2:g.15797C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.932C>G MANE Select	ENSP00000302967.3:p.Thr311Arg
ENST00000305264.7:c.932C>G	ENSP00000302967.3:p.Thr311Arg
ENST00000459727.5:n.233+134C>G
ENST00000467533.5:n.599+134C>G
ENST00000469207.5:n.11C>G
ENST00000469550.6:n.1005C>G
ENST00000475549.1:n.263C>G
ENST00000486618.1:n.426C>G
ENST00000491581.5:n.146C>G
ENST00000492407.1:n.767+134C>G
NM_003883.3:c.932C>G	NP_003874.2:p.Thr311Arg
XM_011537697.1:c.371C>G	XP_011535999.1:p.Thr124Arg
XR_944336.1:n.1017C>G
NM_001355039.1:c.932C>G	NP_001341968.1:p.Thr311Arg
NM_001355040.1:c.473C>G	NP_001341969.1:p.Thr158Arg
NM_001355041.1:c.371C>G	NP_001341970.1:p.Thr124Arg
NR_149164.1:n.998C>G
NR_149165.1:n.880C>G
NR_149166.1:n.843+134C>G
NR_149167.1:n.1011+134C>G
NR_149168.1:n.1023C>G
NR_149169.1:n.1023C>G
NM_003883.4:c.932C>G MANE Select	NP_003874.2:p.Thr311Arg
NM_001355039.2:c.932C>G	NP_001341968.1:p.Thr311Arg
NR_149167.2:n.1004+134C>G
NM_001355040.2:c.473C>G	NP_001341969.1:p.Thr158Arg
NM_001355041.2:c.371C>G	NP_001341970.1:p.Thr124Arg
NR_149164.2:n.991C>G
NR_149165.2:n.873C>G
NR_149166.2:n.836+134C>G
NR_149168.2:n.1016C>G
NR_149169.2:n.1016C>G