Canonical Allele Identifier: CA128439735

Gene: HDAC3

Linked Data

• dbSNP Id: rs1044502334
• gnomAD v3: 5-141624883-A-G
• gnomAD v4: 5-141624883-A-G
• MyVariant Identifiers: chr5:g.141004450A>G (hg19) ; chr5:g.141624883A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624883A>G , CM000667.2:g.141624883A>G	GRCh38
NC_000005.9:g.141004450A>G , CM000667.1:g.141004450A>G	GRCh37
NC_000005.8:g.140984634A>G	NCBI36
NG_029678.1:g.16974T>C
NG_029678.2:g.16974T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.1217+325T>C MANE Select	ENSP00000302967.3:n.1217+325T>C
ENST00000305264.7:c.1217+325T>C	ENSP00000302967.3:n.1217+325T>C
ENST00000459727.5:n.471+325T>C
ENST00000469207.5:n.216+325T>C
ENST00000469550.6:n.1290+325T>C
ENST00000491581.5:n.756T>C
NM_003883.3:c.1217+325T>C	NP_003874.2:n.1217+325T>C
XM_011537697.1:c.656+325T>C	XP_011535999.1:n.656+325T>C
XR_427789.2:n.231-964A>G
XR_944336.1:n.1302+325T>C
NM_001355039.1:c.*237T>C	NP_001341968.1:n.*237T>C
NM_001355040.1:c.758+325T>C	NP_001341969.1:n.758+325T>C
NM_001355041.1:c.656+325T>C	NP_001341970.1:n.656+325T>C
NR_149164.1:n.1203+325T>C
NR_149165.1:n.1165+325T>C
NR_149166.1:n.1081+325T>C
NR_149167.1:n.1574T>C
NR_149168.1:n.1308+325T>C
NR_149169.1:n.1228+325T>C
NM_003883.4:c.1217+325T>C MANE Select	NP_003874.2:n.1217+325T>C
NM_001355039.2:c.*237T>C	NP_001341968.1:n.*237T>C
NR_149167.2:n.1567T>C
NM_001355040.2:c.758+325T>C	NP_001341969.1:n.758+325T>C
NM_001355041.2:c.656+325T>C	NP_001341970.1:n.656+325T>C
NR_149164.2:n.1196+325T>C
NR_149165.2:n.1158+325T>C
NR_149166.2:n.1074+325T>C
NR_149168.2:n.1301+325T>C
NR_149169.2:n.1221+325T>C