Canonical Allele Identifier: CA1587282481
Gene: HDAC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141626125T= , CM000667.2:g.141626125T= GRCh38
NC_000005.9:g.141005692T= , CM000667.1:g.141005692T= GRCh37
NC_000005.8:g.140985876T= NCBI36
NG_029678.1:g.15732A=
NG_029678.2:g.15732A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.921-54A= MANE Select ENSP00000302967.3:n.921-54A=
ENST00000305264.7:c.921-54A= ENSP00000302967.3:n.921-54A=
ENST00000459727.5:n.233+69A=
ENST00000467533.5:n.599+69A=
ENST00000469550.6:n.994-54A=
ENST00000475549.1:n.252-54A=
ENST00000486618.1:n.361A=
ENST00000491581.5:n.135-54A=
ENST00000492407.1:n.767+69A=
NM_003883.3:c.921-54A= NP_003874.2:n.921-54A=
XM_011537697.1:c.360-54A= XP_011535999.1:n.360-54A=
XR_944336.1:n.1006-54A=
NM_001355039.1:c.921-54A= NP_001341968.1:n.921-54A=
NM_001355040.1:c.462-54A= NP_001341969.1:n.462-54A=
NM_001355041.1:c.360-54A= NP_001341970.1:n.360-54A=
NR_149164.1:n.987-54A=
NR_149165.1:n.869-54A=
NR_149166.1:n.843+69A=
NR_149167.1:n.1011+69A=
NR_149168.1:n.1012-54A=
NR_149169.1:n.1012-54A=
NM_003883.4:c.921-54A= MANE Select NP_003874.2:n.921-54A=
NM_001355039.2:c.921-54A= NP_001341968.1:n.921-54A=
NR_149167.2:n.1004+69A=
NM_001355040.2:c.462-54A= NP_001341969.1:n.462-54A=
NM_001355041.2:c.360-54A= NP_001341970.1:n.360-54A=
NR_149164.2:n.980-54A=
NR_149165.2:n.862-54A=
NR_149166.2:n.836+69A=
NR_149168.2:n.1005-54A=
NR_149169.2:n.1005-54A=