Canonical Allele Identifier: CA361515447
Gene: HDAC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.141626058A>T , CM000667.2:g.141626058A>T GRCh38
NC_000005.9:g.141005625A>T , CM000667.1:g.141005625A>T GRCh37
NC_000005.8:g.140985809A>T NCBI36
NG_029678.1:g.15799T>A
NG_029678.2:g.15799T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000305264.8:c.934T>A MANE Select ENSP00000302967.3:p.Ser312Thr
ENST00000305264.7:c.934T>A ENSP00000302967.3:p.Ser312Thr
ENST00000459727.5:n.233+136T>A
ENST00000467533.5:n.599+136T>A
ENST00000469207.5:n.13T>A
ENST00000469550.6:n.1007T>A
ENST00000475549.1:n.265T>A
ENST00000486618.1:n.428T>A
ENST00000491581.5:n.148T>A
ENST00000492407.1:n.767+136T>A
NM_003883.3:c.934T>A NP_003874.2:p.Ser312Thr
XM_011537697.1:c.373T>A XP_011535999.1:p.Ser125Thr
XR_944336.1:n.1019T>A
NM_001355039.1:c.934T>A NP_001341968.1:p.Ser312Thr
NM_001355040.1:c.475T>A NP_001341969.1:p.Ser159Thr
NM_001355041.1:c.373T>A NP_001341970.1:p.Ser125Thr
NR_149164.1:n.1000T>A
NR_149165.1:n.882T>A
NR_149166.1:n.843+136T>A
NR_149167.1:n.1011+136T>A
NR_149168.1:n.1025T>A
NR_149169.1:n.1025T>A
NM_003883.4:c.934T>A MANE Select NP_003874.2:p.Ser312Thr
NM_001355039.2:c.934T>A NP_001341968.1:p.Ser312Thr
NR_149167.2:n.1004+136T>A
NM_001355040.2:c.475T>A NP_001341969.1:p.Ser159Thr
NM_001355041.2:c.373T>A NP_001341970.1:p.Ser125Thr
NR_149164.2:n.993T>A
NR_149165.2:n.875T>A
NR_149166.2:n.836+136T>A
NR_149168.2:n.1018T>A
NR_149169.2:n.1018T>A