Canonical Allele Identifier: CA361515056

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005591A>G (hg19) ; chr5:g.141626024A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626024A>G , CM000667.2:g.141626024A>G	GRCh38
NC_000005.9:g.141005591A>G , CM000667.1:g.141005591A>G	GRCh37
NC_000005.8:g.140985775A>G	NCBI36
NG_029678.1:g.15833T>C
NG_029678.2:g.15833T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.968T>C MANE Select	ENSP00000302967.3:p.Leu323Pro
ENST00000305264.7:c.968T>C	ENSP00000302967.3:p.Leu323Pro
ENST00000459727.5:n.233+170T>C
ENST00000467533.5:n.599+170T>C
ENST00000469207.5:n.47T>C
ENST00000469550.6:n.1041T>C
ENST00000486618.1:n.462T>C
ENST00000491581.5:n.182T>C
ENST00000492407.1:n.767+170T>C
NM_003883.3:c.968T>C	NP_003874.2:p.Leu323Pro
XM_011537697.1:c.407T>C	XP_011535999.1:p.Leu136Pro
XR_944336.1:n.1053T>C
NM_001355039.1:c.968T>C	NP_001341968.1:p.Leu323Pro
NM_001355040.1:c.509T>C	NP_001341969.1:p.Leu170Pro
NM_001355041.1:c.407T>C	NP_001341970.1:p.Leu136Pro
NR_149164.1:n.1034T>C
NR_149165.1:n.916T>C
NR_149166.1:n.843+170T>C
NR_149167.1:n.1011+170T>C
NR_149168.1:n.1059T>C
NR_149169.1:n.1059T>C
NM_003883.4:c.968T>C MANE Select	NP_003874.2:p.Leu323Pro
NM_001355039.2:c.968T>C	NP_001341968.1:p.Leu323Pro
NR_149167.2:n.1004+170T>C
NM_001355040.2:c.509T>C	NP_001341969.1:p.Leu170Pro
NM_001355041.2:c.407T>C	NP_001341970.1:p.Leu136Pro
NR_149164.2:n.1027T>C
NR_149165.2:n.909T>C
NR_149166.2:n.836+170T>C
NR_149168.2:n.1052T>C
NR_149169.2:n.1052T>C