Canonical Allele Identifier: CA446894694

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005658G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626091G>T , CM000667.2:g.141626091G>T	GRCh38
NC_000005.9:g.141005658G>T , CM000667.1:g.141005658G>T	GRCh37
NC_000005.8:g.140985842G>T	NCBI36
NG_029678.1:g.15766C>A
NG_029678.2:g.15766C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.921-20C>A MANE Select	ENSP00000302967.3:n.921-20C>A
ENST00000305264.7:c.921-20C>A	ENSP00000302967.3:n.921-20C>A
ENST00000459727.5:n.233+103C>A
ENST00000467533.5:n.599+103C>A
ENST00000469550.6:n.994-20C>A
ENST00000475549.1:n.252-20C>A
ENST00000486618.1:n.395C>A
ENST00000491581.5:n.135-20C>A
ENST00000492407.1:n.767+103C>A
NM_003883.3:c.921-20C>A	NP_003874.2:n.921-20C>A
XM_011537697.1:c.360-20C>A	XP_011535999.1:n.360-20C>A
XR_944336.1:n.1006-20C>A
NM_001355039.1:c.921-20C>A	NP_001341968.1:n.921-20C>A
NM_001355040.1:c.462-20C>A	NP_001341969.1:n.462-20C>A
NM_001355041.1:c.360-20C>A	NP_001341970.1:n.360-20C>A
NR_149164.1:n.987-20C>A
NR_149165.1:n.869-20C>A
NR_149166.1:n.843+103C>A
NR_149167.1:n.1011+103C>A
NR_149168.1:n.1012-20C>A
NR_149169.1:n.1012-20C>A
NM_003883.4:c.921-20C>A MANE Select	NP_003874.2:n.921-20C>A
NM_001355039.2:c.921-20C>A	NP_001341968.1:n.921-20C>A
NR_149167.2:n.1004+103C>A
NM_001355040.2:c.462-20C>A	NP_001341969.1:n.462-20C>A
NM_001355041.2:c.360-20C>A	NP_001341970.1:n.360-20C>A
NR_149164.2:n.980-20C>A
NR_149165.2:n.862-20C>A
NR_149166.2:n.836+103C>A
NR_149168.2:n.1005-20C>A
NR_149169.2:n.1005-20C>A