Canonical Allele Identifier: CA1587282009
Gene: HDAC3 HGNC NCBI

Linked Data

dbSNP Id: rs2099904239

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141624865G>A , CM000667.2:g.141624865G>A GRCh38
NC_000005.9:g.141004432G>A , CM000667.1:g.141004432G>A GRCh37
NC_000005.8:g.140984616G>A NCBI36
NG_029678.1:g.16992C>T
NG_029678.2:g.16992C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.1217+343C>T MANE Select ENSP00000302967.3:n.1217+343C>T
ENST00000305264.7:c.1217+343C>T ENSP00000302967.3:n.1217+343C>T
ENST00000459727.5:n.471+343C>T
ENST00000469207.5:n.216+343C>T
ENST00000469550.6:n.1290+343C>T
ENST00000491581.5:n.774C>T
NM_003883.3:c.1217+343C>T NP_003874.2:n.1217+343C>T
XM_011537697.1:c.656+343C>T XP_011535999.1:n.656+343C>T
XR_427789.2:n.231-982G>A
XR_944336.1:n.1302+343C>T
NM_001355039.1:c.*255C>T NP_001341968.1:n.*255C>T
NM_001355040.1:c.758+343C>T NP_001341969.1:n.758+343C>T
NM_001355041.1:c.656+343C>T NP_001341970.1:n.656+343C>T
NR_149164.1:n.1203+343C>T
NR_149165.1:n.1165+343C>T
NR_149166.1:n.1081+343C>T
NR_149167.1:n.1592C>T
NR_149168.1:n.1308+343C>T
NR_149169.1:n.1228+343C>T
NM_003883.4:c.1217+343C>T MANE Select NP_003874.2:n.1217+343C>T
NM_001355039.2:c.*255C>T NP_001341968.1:n.*255C>T
NR_149167.2:n.1585C>T
NM_001355040.2:c.758+343C>T NP_001341969.1:n.758+343C>T
NM_001355041.2:c.656+343C>T NP_001341970.1:n.656+343C>T
NR_149164.2:n.1196+343C>T
NR_149165.2:n.1158+343C>T
NR_149166.2:n.1074+343C>T
NR_149168.2:n.1301+343C>T
NR_149169.2:n.1221+343C>T