Canonical Allele Identifier: CA2675696195

Gene: HDAC3

Linked Data

• gnomAD v4: 5-141624767-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624767T>G , CM000667.2:g.141624767T>G	GRCh38
NC_000005.9:g.141004334T>G , CM000667.1:g.141004334T>G	GRCh37
NC_000005.8:g.140984518T>G	NCBI36
NG_029678.1:g.17090A>C
NG_029678.2:g.17090A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000305264.8:c.1217+441A>C MANE Select	ENSP00000302967.3:n.1217+441A>C
ENST00000305264.7:c.1217+441A>C	ENSP00000302967.3:n.1217+441A>C
ENST00000459727.5:n.471+441A>C
ENST00000469207.5:n.216+441A>C
ENST00000469550.6:n.1290+441A>C
NM_003883.3:c.1217+441A>C	NP_003874.2:n.1217+441A>C
XM_011537697.1:c.656+441A>C	XP_011535999.1:n.656+441A>C
XR_427789.2:n.231-1080T>G
XR_944336.1:n.1302+441A>C
NM_001355040.1:c.758+441A>C	NP_001341969.1:n.758+441A>C
NM_001355041.1:c.656+441A>C	NP_001341970.1:n.656+441A>C
NR_149164.1:n.1203+441A>C
NR_149165.1:n.1165+441A>C
NR_149166.1:n.1081+441A>C
NR_149168.1:n.1308+441A>C
NR_149169.1:n.1228+441A>C
NM_003883.4:c.1217+441A>C MANE Select	NP_003874.2:n.1217+441A>C
NM_001355040.2:c.758+441A>C	NP_001341969.1:n.758+441A>C
NM_001355041.2:c.656+441A>C	NP_001341970.1:n.656+441A>C
NR_149164.2:n.1196+441A>C
NR_149165.2:n.1158+441A>C
NR_149166.2:n.1074+441A>C
NR_149168.2:n.1301+441A>C
NR_149169.2:n.1221+441A>C