Canonical Allele Identifier: CA361515203

Gene: HDAC3

Linked Data

• dbSNP Id: rs2099904391
• MyVariant Identifiers: chr5:g.141005604T>C (hg19) ; chr5:g.141626037T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626037T>C , CM000667.2:g.141626037T>C	GRCh38
NC_000005.9:g.141005604T>C , CM000667.1:g.141005604T>C	GRCh37
NC_000005.8:g.140985788T>C	NCBI36
NG_029678.1:g.15820A>G
NG_029678.2:g.15820A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.955A>G MANE Select	ENSP00000302967.3:p.Ile319Val
ENST00000305264.7:c.955A>G	ENSP00000302967.3:p.Ile319Val
ENST00000459727.5:n.233+157A>G
ENST00000467533.5:n.599+157A>G
ENST00000469207.5:n.34A>G
ENST00000469550.6:n.1028A>G
ENST00000475549.1:n.286A>G
ENST00000486618.1:n.449A>G
ENST00000491581.5:n.169A>G
ENST00000492407.1:n.767+157A>G
NM_003883.3:c.955A>G	NP_003874.2:p.Ile319Val
XM_011537697.1:c.394A>G	XP_011535999.1:p.Ile132Val
XR_944336.1:n.1040A>G
NM_001355039.1:c.955A>G	NP_001341968.1:p.Ile319Val
NM_001355040.1:c.496A>G	NP_001341969.1:p.Ile166Val
NM_001355041.1:c.394A>G	NP_001341970.1:p.Ile132Val
NR_149164.1:n.1021A>G
NR_149165.1:n.903A>G
NR_149166.1:n.843+157A>G
NR_149167.1:n.1011+157A>G
NR_149168.1:n.1046A>G
NR_149169.1:n.1046A>G
NM_003883.4:c.955A>G MANE Select	NP_003874.2:p.Ile319Val
NM_001355039.2:c.955A>G	NP_001341968.1:p.Ile319Val
NR_149167.2:n.1004+157A>G
NM_001355040.2:c.496A>G	NP_001341969.1:p.Ile166Val
NM_001355041.2:c.394A>G	NP_001341970.1:p.Ile132Val
NR_149164.2:n.1014A>G
NR_149165.2:n.896A>G
NR_149166.2:n.836+157A>G
NR_149168.2:n.1039A>G
NR_149169.2:n.1039A>G