Canonical Allele Identifier: CA361515138

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005599A>C (hg19) ; chr5:g.141626032A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626032A>C , CM000667.2:g.141626032A>C	GRCh38
NC_000005.9:g.141005599A>C , CM000667.1:g.141005599A>C	GRCh37
NC_000005.8:g.140985783A>C	NCBI36
NG_029678.1:g.15825T>G
NG_029678.2:g.15825T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.960T>G MANE Select	ENSP00000302967.3:p.Ser320Arg
ENST00000305264.7:c.960T>G	ENSP00000302967.3:p.Ser320Arg
ENST00000459727.5:n.233+162T>G
ENST00000467533.5:n.599+162T>G
ENST00000469207.5:n.39T>G
ENST00000469550.6:n.1033T>G
ENST00000475549.1:n.291T>G
ENST00000486618.1:n.454T>G
ENST00000491581.5:n.174T>G
ENST00000492407.1:n.767+162T>G
NM_003883.3:c.960T>G	NP_003874.2:p.Ser320Arg
XM_011537697.1:c.399T>G	XP_011535999.1:p.Ser133Arg
XR_944336.1:n.1045T>G
NM_001355039.1:c.960T>G	NP_001341968.1:p.Ser320Arg
NM_001355040.1:c.501T>G	NP_001341969.1:p.Ser167Arg
NM_001355041.1:c.399T>G	NP_001341970.1:p.Ser133Arg
NR_149164.1:n.1026T>G
NR_149165.1:n.908T>G
NR_149166.1:n.843+162T>G
NR_149167.1:n.1011+162T>G
NR_149168.1:n.1051T>G
NR_149169.1:n.1051T>G
NM_003883.4:c.960T>G MANE Select	NP_003874.2:p.Ser320Arg
NM_001355039.2:c.960T>G	NP_001341968.1:p.Ser320Arg
NR_149167.2:n.1004+162T>G
NM_001355040.2:c.501T>G	NP_001341969.1:p.Ser167Arg
NM_001355041.2:c.399T>G	NP_001341970.1:p.Ser133Arg
NR_149164.2:n.1019T>G
NR_149165.2:n.901T>G
NR_149166.2:n.836+162T>G
NR_149168.2:n.1044T>G
NR_149169.2:n.1044T>G