Canonical Allele Identifier: CA446894539

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005620C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626053C>G , CM000667.2:g.141626053C>G	GRCh38
NC_000005.9:g.141005620C>G , CM000667.1:g.141005620C>G	GRCh37
NC_000005.8:g.140985804C>G	NCBI36
NG_029678.1:g.15804G>C
NG_029678.2:g.15804G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.939G>C MANE Select	ENSP00000302967.3:p.Leu313=
ENST00000305264.7:c.939G>C	ENSP00000302967.3:p.Leu313=
ENST00000459727.5:n.233+141G>C
ENST00000467533.5:n.599+141G>C
ENST00000469207.5:n.18G>C
ENST00000469550.6:n.1012G>C
ENST00000475549.1:n.270G>C
ENST00000486618.1:n.433G>C
ENST00000491581.5:n.153G>C
ENST00000492407.1:n.767+141G>C
NM_003883.3:c.939G>C	NP_003874.2:p.Leu313=
XM_011537697.1:c.378G>C	XP_011535999.1:p.Leu126=
XR_944336.1:n.1024G>C
NM_001355039.1:c.939G>C	NP_001341968.1:p.Leu313=
NM_001355040.1:c.480G>C	NP_001341969.1:p.Leu160=
NM_001355041.1:c.378G>C	NP_001341970.1:p.Leu126=
NR_149164.1:n.1005G>C
NR_149165.1:n.887G>C
NR_149166.1:n.843+141G>C
NR_149167.1:n.1011+141G>C
NR_149168.1:n.1030G>C
NR_149169.1:n.1030G>C
NM_003883.4:c.939G>C MANE Select	NP_003874.2:p.Leu313=
NM_001355039.2:c.939G>C	NP_001341968.1:p.Leu313=
NR_149167.2:n.1004+141G>C
NM_001355040.2:c.480G>C	NP_001341969.1:p.Leu160=
NM_001355041.2:c.378G>C	NP_001341970.1:p.Leu126=
NR_149164.2:n.998G>C
NR_149165.2:n.880G>C
NR_149166.2:n.836+141G>C
NR_149168.2:n.1023G>C
NR_149169.2:n.1023G>C