Canonical Allele Identifier: CA2675696258

Gene: HDAC3

Linked Data

• gnomAD v4: 5-141624901-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141624901G>T , CM000667.2:g.141624901G>T	GRCh38
NC_000005.9:g.141004468G>T , CM000667.1:g.141004468G>T	GRCh37
NC_000005.8:g.140984652G>T	NCBI36
NG_029678.1:g.16956C>A
NG_029678.2:g.16956C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.1217+307C>A MANE Select	ENSP00000302967.3:n.1217+307C>A
ENST00000305264.7:c.1217+307C>A	ENSP00000302967.3:n.1217+307C>A
ENST00000459727.5:n.471+307C>A
ENST00000469207.5:n.216+307C>A
ENST00000469550.6:n.1290+307C>A
ENST00000491581.5:n.738C>A
NM_003883.3:c.1217+307C>A	NP_003874.2:n.1217+307C>A
XM_011537697.1:c.656+307C>A	XP_011535999.1:n.656+307C>A
XR_427789.2:n.231-946G>T
XR_944336.1:n.1302+307C>A
NM_001355039.1:c.*219C>A	NP_001341968.1:n.*219C>A
NM_001355040.1:c.758+307C>A	NP_001341969.1:n.758+307C>A
NM_001355041.1:c.656+307C>A	NP_001341970.1:n.656+307C>A
NR_149164.1:n.1203+307C>A
NR_149165.1:n.1165+307C>A
NR_149166.1:n.1081+307C>A
NR_149167.1:n.1556C>A
NR_149168.1:n.1308+307C>A
NR_149169.1:n.1228+307C>A
NM_003883.4:c.1217+307C>A MANE Select	NP_003874.2:n.1217+307C>A
NM_001355039.2:c.*219C>A	NP_001341968.1:n.*219C>A
NR_149167.2:n.1549C>A
NM_001355040.2:c.758+307C>A	NP_001341969.1:n.758+307C>A
NM_001355041.2:c.656+307C>A	NP_001341970.1:n.656+307C>A
NR_149164.2:n.1196+307C>A
NR_149165.2:n.1158+307C>A
NR_149166.2:n.1074+307C>A
NR_149168.2:n.1301+307C>A
NR_149169.2:n.1221+307C>A