Canonical Allele Identifier: CA361515555

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005636G>T (hg19) ; chr5:g.141626069G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626069G>T , CM000667.2:g.141626069G>T	GRCh38
NC_000005.9:g.141005636G>T , CM000667.1:g.141005636G>T	GRCh37
NC_000005.8:g.140985820G>T	NCBI36
NG_029678.1:g.15788C>A
NG_029678.2:g.15788C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.923C>A MANE Select	ENSP00000302967.3:p.Thr308Lys
ENST00000305264.7:c.923C>A	ENSP00000302967.3:p.Thr308Lys
ENST00000459727.5:n.233+125C>A
ENST00000467533.5:n.599+125C>A
ENST00000469207.5:n.2C>A
ENST00000469550.6:n.996C>A
ENST00000475549.1:n.254C>A
ENST00000486618.1:n.417C>A
ENST00000491581.5:n.137C>A
ENST00000492407.1:n.767+125C>A
NM_003883.3:c.923C>A	NP_003874.2:p.Thr308Lys
XM_011537697.1:c.362C>A	XP_011535999.1:p.Thr121Lys
XR_944336.1:n.1008C>A
NM_001355039.1:c.923C>A	NP_001341968.1:p.Thr308Lys
NM_001355040.1:c.464C>A	NP_001341969.1:p.Thr155Lys
NM_001355041.1:c.362C>A	NP_001341970.1:p.Thr121Lys
NR_149164.1:n.989C>A
NR_149165.1:n.871C>A
NR_149166.1:n.843+125C>A
NR_149167.1:n.1011+125C>A
NR_149168.1:n.1014C>A
NR_149169.1:n.1014C>A
NM_003883.4:c.923C>A MANE Select	NP_003874.2:p.Thr308Lys
NM_001355039.2:c.923C>A	NP_001341968.1:p.Thr308Lys
NR_149167.2:n.1004+125C>A
NM_001355040.2:c.464C>A	NP_001341969.1:p.Thr155Lys
NM_001355041.2:c.362C>A	NP_001341970.1:p.Thr121Lys
NR_149164.2:n.982C>A
NR_149165.2:n.864C>A
NR_149166.2:n.836+125C>A
NR_149168.2:n.1007C>A
NR_149169.2:n.1007C>A