Canonical Allele Identifier: CA2675696236

Gene: HDAC3

Linked Data

• gnomAD v4: 5-141624840-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624845del , CM000667.2:g.141624845del	GRCh38
NC_000005.9:g.141004412del , CM000667.1:g.141004412del	GRCh37
NC_000005.8:g.140984596del	NCBI36
NG_029678.1:g.17016del
NG_029678.2:g.17016del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.1217+367del MANE Select	ENSP00000302967.3:n.1217+367del
ENST00000305264.7:c.1217+367del	ENSP00000302967.3:n.1217+367del
ENST00000459727.5:n.471+367del
ENST00000469207.5:n.216+367del
ENST00000469550.6:n.1290+367del
NM_003883.3:c.1217+367del	NP_003874.2:n.1217+367del
XM_011537697.1:c.656+367del	XP_011535999.1:n.656+367del
XR_427789.2:n.231-1002del
XR_944336.1:n.1302+367del
NM_001355040.1:c.758+367del	NP_001341969.1:n.758+367del
NM_001355041.1:c.656+367del	NP_001341970.1:n.656+367del
NR_149164.1:n.1203+367del
NR_149165.1:n.1165+367del
NR_149166.1:n.1081+367del
NR_149168.1:n.1308+367del
NR_149169.1:n.1228+367del
NM_003883.4:c.1217+367del MANE Select	NP_003874.2:n.1217+367del
NM_001355040.2:c.758+367del	NP_001341969.1:n.758+367del
NM_001355041.2:c.656+367del	NP_001341970.1:n.656+367del
NR_149164.2:n.1196+367del
NR_149165.2:n.1158+367del
NR_149166.2:n.1074+367del
NR_149168.2:n.1301+367del
NR_149169.2:n.1221+367del