Canonical Allele Identifier: CA2675696800

Gene: HDAC3

Linked Data

• gnomAD v4: 5-141626081-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626083del , CM000667.2:g.141626083del	GRCh38
NC_000005.9:g.141005650del , CM000667.1:g.141005650del	GRCh37
NC_000005.8:g.140985834del	NCBI36
NG_029678.1:g.15775del
NG_029678.2:g.15775del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.921-11del MANE Select	ENSP00000302967.3:n.921-11del
ENST00000305264.7:c.921-11del	ENSP00000302967.3:n.921-11del
ENST00000459727.5:n.233+112del
ENST00000467533.5:n.599+112del
ENST00000469550.6:n.994-11del
ENST00000475549.1:n.252-11del
ENST00000486618.1:n.404del
ENST00000491581.5:n.135-11del
ENST00000492407.1:n.767+112del
NM_003883.3:c.921-11del	NP_003874.2:n.921-11del
XM_011537697.1:c.360-11del	XP_011535999.1:n.360-11del
XR_944336.1:n.1006-11del
NM_001355039.1:c.921-11del	NP_001341968.1:n.921-11del
NM_001355040.1:c.462-11del	NP_001341969.1:n.462-11del
NM_001355041.1:c.360-11del	NP_001341970.1:n.360-11del
NR_149164.1:n.987-11del
NR_149165.1:n.869-11del
NR_149166.1:n.843+112del
NR_149167.1:n.1011+112del
NR_149168.1:n.1012-11del
NR_149169.1:n.1012-11del
NM_003883.4:c.921-11del MANE Select	NP_003874.2:n.921-11del
NM_001355039.2:c.921-11del	NP_001341968.1:n.921-11del
NR_149167.2:n.1004+112del
NM_001355040.2:c.462-11del	NP_001341969.1:n.462-11del
NM_001355041.2:c.360-11del	NP_001341970.1:n.360-11del
NR_149164.2:n.980-11del
NR_149165.2:n.862-11del
NR_149166.2:n.836+112del
NR_149168.2:n.1005-11del
NR_149169.2:n.1005-11del