Canonical Allele Identifier: CA2675696214

Gene: HDAC3

Linked Data

• gnomAD v4: 5-141624802-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624802G>T , CM000667.2:g.141624802G>T	GRCh38
NC_000005.9:g.141004369G>T , CM000667.1:g.141004369G>T	GRCh37
NC_000005.8:g.140984553G>T	NCBI36
NG_029678.1:g.17055C>A
NG_029678.2:g.17055C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.1217+406C>A MANE Select	ENSP00000302967.3:n.1217+406C>A
ENST00000305264.7:c.1217+406C>A	ENSP00000302967.3:n.1217+406C>A
ENST00000459727.5:n.471+406C>A
ENST00000469207.5:n.216+406C>A
ENST00000469550.6:n.1290+406C>A
NM_003883.3:c.1217+406C>A	NP_003874.2:n.1217+406C>A
XM_011537697.1:c.656+406C>A	XP_011535999.1:n.656+406C>A
XR_427789.2:n.231-1045G>T
XR_944336.1:n.1302+406C>A
NM_001355040.1:c.758+406C>A	NP_001341969.1:n.758+406C>A
NM_001355041.1:c.656+406C>A	NP_001341970.1:n.656+406C>A
NR_149164.1:n.1203+406C>A
NR_149165.1:n.1165+406C>A
NR_149166.1:n.1081+406C>A
NR_149168.1:n.1308+406C>A
NR_149169.1:n.1228+406C>A
NM_003883.4:c.1217+406C>A MANE Select	NP_003874.2:n.1217+406C>A
NM_001355040.2:c.758+406C>A	NP_001341969.1:n.758+406C>A
NM_001355041.2:c.656+406C>A	NP_001341970.1:n.656+406C>A
NR_149164.2:n.1196+406C>A
NR_149165.2:n.1158+406C>A
NR_149166.2:n.1074+406C>A
NR_149168.2:n.1301+406C>A
NR_149169.2:n.1221+406C>A