Canonical Allele Identifier: CA361515543

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005634A>C (hg19) ; chr5:g.141626067A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626067A>C , CM000667.2:g.141626067A>C	GRCh38
NC_000005.9:g.141005634A>C , CM000667.1:g.141005634A>C	GRCh37
NC_000005.8:g.140985818A>C	NCBI36
NG_029678.1:g.15790T>G
NG_029678.2:g.15790T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.925T>G MANE Select	ENSP00000302967.3:p.Tyr309Asp
ENST00000305264.7:c.925T>G	ENSP00000302967.3:p.Tyr309Asp
ENST00000459727.5:n.233+127T>G
ENST00000467533.5:n.599+127T>G
ENST00000469207.5:n.4T>G
ENST00000469550.6:n.998T>G
ENST00000475549.1:n.256T>G
ENST00000486618.1:n.419T>G
ENST00000491581.5:n.139T>G
ENST00000492407.1:n.767+127T>G
NM_003883.3:c.925T>G	NP_003874.2:p.Tyr309Asp
XM_011537697.1:c.364T>G	XP_011535999.1:p.Tyr122Asp
XR_944336.1:n.1010T>G
NM_001355039.1:c.925T>G	NP_001341968.1:p.Tyr309Asp
NM_001355040.1:c.466T>G	NP_001341969.1:p.Tyr156Asp
NM_001355041.1:c.364T>G	NP_001341970.1:p.Tyr122Asp
NR_149164.1:n.991T>G
NR_149165.1:n.873T>G
NR_149166.1:n.843+127T>G
NR_149167.1:n.1011+127T>G
NR_149168.1:n.1016T>G
NR_149169.1:n.1016T>G
NM_003883.4:c.925T>G MANE Select	NP_003874.2:p.Tyr309Asp
NM_001355039.2:c.925T>G	NP_001341968.1:p.Tyr309Asp
NR_149167.2:n.1004+127T>G
NM_001355040.2:c.466T>G	NP_001341969.1:p.Tyr156Asp
NM_001355041.2:c.364T>G	NP_001341970.1:p.Tyr122Asp
NR_149164.2:n.984T>G
NR_149165.2:n.866T>G
NR_149166.2:n.836+127T>G
NR_149168.2:n.1009T>G
NR_149169.2:n.1009T>G