Canonical Allele Identifier: CA446894606

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005635T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626068T>G , CM000667.2:g.141626068T>G	GRCh38
NC_000005.9:g.141005635T>G , CM000667.1:g.141005635T>G	GRCh37
NC_000005.8:g.140985819T>G	NCBI36
NG_029678.1:g.15789A>C
NG_029678.2:g.15789A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.924A>C MANE Select	ENSP00000302967.3:p.Thr308=
ENST00000305264.7:c.924A>C	ENSP00000302967.3:p.Thr308=
ENST00000459727.5:n.233+126A>C
ENST00000467533.5:n.599+126A>C
ENST00000469207.5:n.3A>C
ENST00000469550.6:n.997A>C
ENST00000475549.1:n.255A>C
ENST00000486618.1:n.418A>C
ENST00000491581.5:n.138A>C
ENST00000492407.1:n.767+126A>C
NM_003883.3:c.924A>C	NP_003874.2:p.Thr308=
XM_011537697.1:c.363A>C	XP_011535999.1:p.Thr121=
XR_944336.1:n.1009A>C
NM_001355039.1:c.924A>C	NP_001341968.1:p.Thr308=
NM_001355040.1:c.465A>C	NP_001341969.1:p.Thr155=
NM_001355041.1:c.363A>C	NP_001341970.1:p.Thr121=
NR_149164.1:n.990A>C
NR_149165.1:n.872A>C
NR_149166.1:n.843+126A>C
NR_149167.1:n.1011+126A>C
NR_149168.1:n.1015A>C
NR_149169.1:n.1015A>C
NM_003883.4:c.924A>C MANE Select	NP_003874.2:p.Thr308=
NM_001355039.2:c.924A>C	NP_001341968.1:p.Thr308=
NR_149167.2:n.1004+126A>C
NM_001355040.2:c.465A>C	NP_001341969.1:p.Thr155=
NM_001355041.2:c.363A>C	NP_001341970.1:p.Thr121=
NR_149164.2:n.983A>C
NR_149165.2:n.865A>C
NR_149166.2:n.836+126A>C
NR_149168.2:n.1008A>C
NR_149169.2:n.1008A>C