Canonical Allele Identifier: CA361515228

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005607C>T (hg19) ; chr5:g.141626040C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626040C>T , CM000667.2:g.141626040C>T	GRCh38
NC_000005.9:g.141005607C>T , CM000667.1:g.141005607C>T	GRCh37
NC_000005.8:g.140985791C>T	NCBI36
NG_029678.1:g.15817G>A
NG_029678.2:g.15817G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.952G>A MANE Select	ENSP00000302967.3:p.Ala318Thr
ENST00000305264.7:c.952G>A	ENSP00000302967.3:p.Ala318Thr
ENST00000459727.5:n.233+154G>A
ENST00000467533.5:n.599+154G>A
ENST00000469207.5:n.31G>A
ENST00000469550.6:n.1025G>A
ENST00000475549.1:n.283G>A
ENST00000486618.1:n.446G>A
ENST00000491581.5:n.166G>A
ENST00000492407.1:n.767+154G>A
NM_003883.3:c.952G>A	NP_003874.2:p.Ala318Thr
XM_011537697.1:c.391G>A	XP_011535999.1:p.Ala131Thr
XR_944336.1:n.1037G>A
NM_001355039.1:c.952G>A	NP_001341968.1:p.Ala318Thr
NM_001355040.1:c.493G>A	NP_001341969.1:p.Ala165Thr
NM_001355041.1:c.391G>A	NP_001341970.1:p.Ala131Thr
NR_149164.1:n.1018G>A
NR_149165.1:n.900G>A
NR_149166.1:n.843+154G>A
NR_149167.1:n.1011+154G>A
NR_149168.1:n.1043G>A
NR_149169.1:n.1043G>A
NM_003883.4:c.952G>A MANE Select	NP_003874.2:p.Ala318Thr
NM_001355039.2:c.952G>A	NP_001341968.1:p.Ala318Thr
NR_149167.2:n.1004+154G>A
NM_001355040.2:c.493G>A	NP_001341969.1:p.Ala165Thr
NM_001355041.2:c.391G>A	NP_001341970.1:p.Ala131Thr
NR_149164.2:n.1011G>A
NR_149165.2:n.893G>A
NR_149166.2:n.836+154G>A
NR_149168.2:n.1036G>A
NR_149169.2:n.1036G>A