Canonical Allele Identifier: CA446894747

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005667C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626100C>G , CM000667.2:g.141626100C>G	GRCh38
NC_000005.9:g.141005667C>G , CM000667.1:g.141005667C>G	GRCh37
NC_000005.8:g.140985851C>G	NCBI36
NG_029678.1:g.15757G>C
NG_029678.2:g.15757G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.921-29G>C MANE Select	ENSP00000302967.3:n.921-29G>C
ENST00000305264.7:c.921-29G>C	ENSP00000302967.3:n.921-29G>C
ENST00000459727.5:n.233+94G>C
ENST00000467533.5:n.599+94G>C
ENST00000469550.6:n.994-29G>C
ENST00000475549.1:n.252-29G>C
ENST00000486618.1:n.386G>C
ENST00000491581.5:n.135-29G>C
ENST00000492407.1:n.767+94G>C
NM_003883.3:c.921-29G>C	NP_003874.2:n.921-29G>C
XM_011537697.1:c.360-29G>C	XP_011535999.1:n.360-29G>C
XR_944336.1:n.1006-29G>C
NM_001355039.1:c.921-29G>C	NP_001341968.1:n.921-29G>C
NM_001355040.1:c.462-29G>C	NP_001341969.1:n.462-29G>C
NM_001355041.1:c.360-29G>C	NP_001341970.1:n.360-29G>C
NR_149164.1:n.987-29G>C
NR_149165.1:n.869-29G>C
NR_149166.1:n.843+94G>C
NR_149167.1:n.1011+94G>C
NR_149168.1:n.1012-29G>C
NR_149169.1:n.1012-29G>C
NM_003883.4:c.921-29G>C MANE Select	NP_003874.2:n.921-29G>C
NM_001355039.2:c.921-29G>C	NP_001341968.1:n.921-29G>C
NR_149167.2:n.1004+94G>C
NM_001355040.2:c.462-29G>C	NP_001341969.1:n.462-29G>C
NM_001355041.2:c.360-29G>C	NP_001341970.1:n.360-29G>C
NR_149164.2:n.980-29G>C
NR_149165.2:n.862-29G>C
NR_149166.2:n.836+94G>C
NR_149168.2:n.1005-29G>C
NR_149169.2:n.1005-29G>C