Canonical Allele Identifier: CA446894808

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005676T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626109T>G , CM000667.2:g.141626109T>G	GRCh38
NC_000005.9:g.141005676T>G , CM000667.1:g.141005676T>G	GRCh37
NC_000005.8:g.140985860T>G	NCBI36
NG_029678.1:g.15748A>C
NG_029678.2:g.15748A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.921-38A>C MANE Select	ENSP00000302967.3:n.921-38A>C
ENST00000305264.7:c.921-38A>C	ENSP00000302967.3:n.921-38A>C
ENST00000459727.5:n.233+85A>C
ENST00000467533.5:n.599+85A>C
ENST00000469550.6:n.994-38A>C
ENST00000475549.1:n.252-38A>C
ENST00000486618.1:n.377A>C
ENST00000491581.5:n.135-38A>C
ENST00000492407.1:n.767+85A>C
NM_003883.3:c.921-38A>C	NP_003874.2:n.921-38A>C
XM_011537697.1:c.360-38A>C	XP_011535999.1:n.360-38A>C
XR_944336.1:n.1006-38A>C
NM_001355039.1:c.921-38A>C	NP_001341968.1:n.921-38A>C
NM_001355040.1:c.462-38A>C	NP_001341969.1:n.462-38A>C
NM_001355041.1:c.360-38A>C	NP_001341970.1:n.360-38A>C
NR_149164.1:n.987-38A>C
NR_149165.1:n.869-38A>C
NR_149166.1:n.843+85A>C
NR_149167.1:n.1011+85A>C
NR_149168.1:n.1012-38A>C
NR_149169.1:n.1012-38A>C
NM_003883.4:c.921-38A>C MANE Select	NP_003874.2:n.921-38A>C
NM_001355039.2:c.921-38A>C	NP_001341968.1:n.921-38A>C
NR_149167.2:n.1004+85A>C
NM_001355040.2:c.462-38A>C	NP_001341969.1:n.462-38A>C
NM_001355041.2:c.360-38A>C	NP_001341970.1:n.360-38A>C
NR_149164.2:n.980-38A>C
NR_149165.2:n.862-38A>C
NR_149166.2:n.836+85A>C
NR_149168.2:n.1005-38A>C
NR_149169.2:n.1005-38A>C