Canonical Allele Identifier: CA128439731

Gene: HDAC3

Linked Data

• dbSNP Id: rs1025327581
• gnomAD v3: 5-141624870-T-C
• gnomAD v4: 5-141624870-T-C
• MyVariant Identifiers: chr5:g.141004437T>C (hg19) ; chr5:g.141624870T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624870T>C , CM000667.2:g.141624870T>C	GRCh38
NC_000005.9:g.141004437T>C , CM000667.1:g.141004437T>C	GRCh37
NC_000005.8:g.140984621T>C	NCBI36
NG_029678.1:g.16987A>G
NG_029678.2:g.16987A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.1217+338A>G MANE Select	ENSP00000302967.3:n.1217+338A>G
ENST00000305264.7:c.1217+338A>G	ENSP00000302967.3:n.1217+338A>G
ENST00000459727.5:n.471+338A>G
ENST00000469207.5:n.216+338A>G
ENST00000469550.6:n.1290+338A>G
ENST00000491581.5:n.769A>G
NM_003883.3:c.1217+338A>G	NP_003874.2:n.1217+338A>G
XM_011537697.1:c.656+338A>G	XP_011535999.1:n.656+338A>G
XR_427789.2:n.231-977T>C
XR_944336.1:n.1302+338A>G
NM_001355039.1:c.*250A>G	NP_001341968.1:n.*250A>G
NM_001355040.1:c.758+338A>G	NP_001341969.1:n.758+338A>G
NM_001355041.1:c.656+338A>G	NP_001341970.1:n.656+338A>G
NR_149164.1:n.1203+338A>G
NR_149165.1:n.1165+338A>G
NR_149166.1:n.1081+338A>G
NR_149167.1:n.1587A>G
NR_149168.1:n.1308+338A>G
NR_149169.1:n.1228+338A>G
NM_003883.4:c.1217+338A>G MANE Select	NP_003874.2:n.1217+338A>G
NM_001355039.2:c.*250A>G	NP_001341968.1:n.*250A>G
NR_149167.2:n.1580A>G
NM_001355040.2:c.758+338A>G	NP_001341969.1:n.758+338A>G
NM_001355041.2:c.656+338A>G	NP_001341970.1:n.656+338A>G
NR_149164.2:n.1196+338A>G
NR_149165.2:n.1158+338A>G
NR_149166.2:n.1074+338A>G
NR_149168.2:n.1301+338A>G
NR_149169.2:n.1221+338A>G