Canonical Allele Identifier: CA2768672819

Gene: HDAC3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624832C>A , CM000667.2:g.141624832C>A	GRCh38
NC_000005.9:g.141004399C>A , CM000667.1:g.141004399C>A	GRCh37
NC_000005.8:g.140984583C>A	NCBI36
NG_029678.1:g.17025G>T
NG_029678.2:g.17025G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.1217+376G>T MANE Select	ENSP00000302967.3:n.1217+376G>T
ENST00000305264.7:c.1217+376G>T	ENSP00000302967.3:n.1217+376G>T
ENST00000459727.5:n.471+376G>T
ENST00000469207.5:n.216+376G>T
ENST00000469550.6:n.1290+376G>T
NM_003883.3:c.1217+376G>T	NP_003874.2:n.1217+376G>T
XM_011537697.1:c.656+376G>T	XP_011535999.1:n.656+376G>T
XR_427789.2:n.231-1015C>A
XR_944336.1:n.1302+376G>T
NM_001355040.1:c.758+376G>T	NP_001341969.1:n.758+376G>T
NM_001355041.1:c.656+376G>T	NP_001341970.1:n.656+376G>T
NR_149164.1:n.1203+376G>T
NR_149165.1:n.1165+376G>T
NR_149166.1:n.1081+376G>T
NR_149168.1:n.1308+376G>T
NR_149169.1:n.1228+376G>T
NM_003883.4:c.1217+376G>T MANE Select	NP_003874.2:n.1217+376G>T
NM_001355040.2:c.758+376G>T	NP_001341969.1:n.758+376G>T
NM_001355041.2:c.656+376G>T	NP_001341970.1:n.656+376G>T
NR_149164.2:n.1196+376G>T
NR_149165.2:n.1158+376G>T
NR_149166.2:n.1074+376G>T
NR_149168.2:n.1301+376G>T
NR_149169.2:n.1221+376G>T