Canonical Allele Identifier: CA446894890
Gene: HDAC3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.141005689C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141626122C>A , CM000667.2:g.141626122C>A GRCh38
NC_000005.9:g.141005689C>A , CM000667.1:g.141005689C>A GRCh37
NC_000005.8:g.140985873C>A NCBI36
NG_029678.1:g.15735G>T
NG_029678.2:g.15735G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.921-51G>T MANE Select ENSP00000302967.3:n.921-51G>T
ENST00000305264.7:c.921-51G>T ENSP00000302967.3:n.921-51G>T
ENST00000459727.5:n.233+72G>T
ENST00000467533.5:n.599+72G>T
ENST00000469550.6:n.994-51G>T
ENST00000475549.1:n.252-51G>T
ENST00000486618.1:n.364G>T
ENST00000491581.5:n.135-51G>T
ENST00000492407.1:n.767+72G>T
NM_003883.3:c.921-51G>T NP_003874.2:n.921-51G>T
XM_011537697.1:c.360-51G>T XP_011535999.1:n.360-51G>T
XR_944336.1:n.1006-51G>T
NM_001355039.1:c.921-51G>T NP_001341968.1:n.921-51G>T
NM_001355040.1:c.462-51G>T NP_001341969.1:n.462-51G>T
NM_001355041.1:c.360-51G>T NP_001341970.1:n.360-51G>T
NR_149164.1:n.987-51G>T
NR_149165.1:n.869-51G>T
NR_149166.1:n.843+72G>T
NR_149167.1:n.1011+72G>T
NR_149168.1:n.1012-51G>T
NR_149169.1:n.1012-51G>T
NM_003883.4:c.921-51G>T MANE Select NP_003874.2:n.921-51G>T
NM_001355039.2:c.921-51G>T NP_001341968.1:n.921-51G>T
NR_149167.2:n.1004+72G>T
NM_001355040.2:c.462-51G>T NP_001341969.1:n.462-51G>T
NM_001355041.2:c.360-51G>T NP_001341970.1:n.360-51G>T
NR_149164.2:n.980-51G>T
NR_149165.2:n.862-51G>T
NR_149166.2:n.836+72G>T
NR_149168.2:n.1005-51G>T
NR_149169.2:n.1005-51G>T