Canonical Allele Identifier: CA361515271
Gene: HDAC3 HGNC NCBI

Linked Data

COSMIC: COSM736587

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141626043C>A , CM000667.2:g.141626043C>A GRCh38
NC_000005.9:g.141005610C>A , CM000667.1:g.141005610C>A GRCh37
NC_000005.8:g.140985794C>A NCBI36
NG_029678.1:g.15814G>T
NG_029678.2:g.15814G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.949G>T MANE Select ENSP00000302967.3:p.Glu317Ter
ENST00000305264.7:c.949G>T ENSP00000302967.3:p.Glu317Ter
ENST00000459727.5:n.233+151G>T
ENST00000467533.5:n.599+151G>T
ENST00000469207.5:n.28G>T
ENST00000469550.6:n.1022G>T
ENST00000475549.1:n.280G>T
ENST00000486618.1:n.443G>T
ENST00000491581.5:n.163G>T
ENST00000492407.1:n.767+151G>T
NM_003883.3:c.949G>T NP_003874.2:p.Glu317Ter
XM_011537697.1:c.388G>T XP_011535999.1:p.Glu130Ter
XR_944336.1:n.1034G>T
NM_001355039.1:c.949G>T NP_001341968.1:p.Glu317Ter
NM_001355040.1:c.490G>T NP_001341969.1:p.Glu164Ter
NM_001355041.1:c.388G>T NP_001341970.1:p.Glu130Ter
NR_149164.1:n.1015G>T
NR_149165.1:n.897G>T
NR_149166.1:n.843+151G>T
NR_149167.1:n.1011+151G>T
NR_149168.1:n.1040G>T
NR_149169.1:n.1040G>T
NM_003883.4:c.949G>T MANE Select NP_003874.2:p.Glu317Ter
NM_001355039.2:c.949G>T NP_001341968.1:p.Glu317Ter
NR_149167.2:n.1004+151G>T
NM_001355040.2:c.490G>T NP_001341969.1:p.Glu164Ter
NM_001355041.2:c.388G>T NP_001341970.1:p.Glu130Ter
NR_149164.2:n.1008G>T
NR_149165.2:n.890G>T
NR_149166.2:n.836+151G>T
NR_149168.2:n.1033G>T
NR_149169.2:n.1033G>T