Canonical Allele Identifier: CA361515079

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005593C>G (hg19) ; chr5:g.141626026C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626026C>G , CM000667.2:g.141626026C>G	GRCh38
NC_000005.9:g.141005593C>G , CM000667.1:g.141005593C>G	GRCh37
NC_000005.8:g.140985777C>G	NCBI36
NG_029678.1:g.15831G>C
NG_029678.2:g.15831G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.966G>C MANE Select	ENSP00000302967.3:p.Glu322Asp
ENST00000305264.7:c.966G>C	ENSP00000302967.3:p.Glu322Asp
ENST00000459727.5:n.233+168G>C
ENST00000467533.5:n.599+168G>C
ENST00000469207.5:n.45G>C
ENST00000469550.6:n.1039G>C
ENST00000475549.1:n.297G>C
ENST00000486618.1:n.460G>C
ENST00000491581.5:n.180G>C
ENST00000492407.1:n.767+168G>C
NM_003883.3:c.966G>C	NP_003874.2:p.Glu322Asp
XM_011537697.1:c.405G>C	XP_011535999.1:p.Glu135Asp
XR_944336.1:n.1051G>C
NM_001355039.1:c.966G>C	NP_001341968.1:p.Glu322Asp
NM_001355040.1:c.507G>C	NP_001341969.1:p.Glu169Asp
NM_001355041.1:c.405G>C	NP_001341970.1:p.Glu135Asp
NR_149164.1:n.1032G>C
NR_149165.1:n.914G>C
NR_149166.1:n.843+168G>C
NR_149167.1:n.1011+168G>C
NR_149168.1:n.1057G>C
NR_149169.1:n.1057G>C
NM_003883.4:c.966G>C MANE Select	NP_003874.2:p.Glu322Asp
NM_001355039.2:c.966G>C	NP_001341968.1:p.Glu322Asp
NR_149167.2:n.1004+168G>C
NM_001355040.2:c.507G>C	NP_001341969.1:p.Glu169Asp
NM_001355041.2:c.405G>C	NP_001341970.1:p.Glu135Asp
NR_149164.2:n.1025G>C
NR_149165.2:n.907G>C
NR_149166.2:n.836+168G>C
NR_149168.2:n.1050G>C
NR_149169.2:n.1050G>C