Canonical Allele Identifier: CA361515153

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005600C>G (hg19) ; chr5:g.141626033C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626033C>G , CM000667.2:g.141626033C>G	GRCh38
NC_000005.9:g.141005600C>G , CM000667.1:g.141005600C>G	GRCh37
NC_000005.8:g.140985784C>G	NCBI36
NG_029678.1:g.15824G>C
NG_029678.2:g.15824G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.959G>C MANE Select	ENSP00000302967.3:p.Ser320Thr
ENST00000305264.7:c.959G>C	ENSP00000302967.3:p.Ser320Thr
ENST00000459727.5:n.233+161G>C
ENST00000467533.5:n.599+161G>C
ENST00000469207.5:n.38G>C
ENST00000469550.6:n.1032G>C
ENST00000475549.1:n.290G>C
ENST00000486618.1:n.453G>C
ENST00000491581.5:n.173G>C
ENST00000492407.1:n.767+161G>C
NM_003883.3:c.959G>C	NP_003874.2:p.Ser320Thr
XM_011537697.1:c.398G>C	XP_011535999.1:p.Ser133Thr
XR_944336.1:n.1044G>C
NM_001355039.1:c.959G>C	NP_001341968.1:p.Ser320Thr
NM_001355040.1:c.500G>C	NP_001341969.1:p.Ser167Thr
NM_001355041.1:c.398G>C	NP_001341970.1:p.Ser133Thr
NR_149164.1:n.1025G>C
NR_149165.1:n.907G>C
NR_149166.1:n.843+161G>C
NR_149167.1:n.1011+161G>C
NR_149168.1:n.1050G>C
NR_149169.1:n.1050G>C
NM_003883.4:c.959G>C MANE Select	NP_003874.2:p.Ser320Thr
NM_001355039.2:c.959G>C	NP_001341968.1:p.Ser320Thr
NR_149167.2:n.1004+161G>C
NM_001355040.2:c.500G>C	NP_001341969.1:p.Ser167Thr
NM_001355041.2:c.398G>C	NP_001341970.1:p.Ser133Thr
NR_149164.2:n.1018G>C
NR_149165.2:n.900G>C
NR_149166.2:n.836+161G>C
NR_149168.2:n.1043G>C
NR_149169.2:n.1043G>C