Canonical Allele Identifier: CA446894509

Gene: HDAC3

Linked Data

• dbSNP Id: rs768270778
• gnomAD v2: 5-141005614-T-A
• gnomAD v4: 5-141626047-T-A
• MyVariant Identifiers: chr5:g.141005614T>A (hg19) ; chr5:g.141626047T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626047T>A , CM000667.2:g.141626047T>A	GRCh38
NC_000005.9:g.141005614T>A , CM000667.1:g.141005614T>A	GRCh37
NC_000005.8:g.140985798T>A	NCBI36
NG_029678.1:g.15810A>T
NG_029678.2:g.15810A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.945A>T MANE Select	ENSP00000302967.3:p.Val315=
ENST00000305264.7:c.945A>T	ENSP00000302967.3:p.Val315=
ENST00000459727.5:n.233+147A>T
ENST00000467533.5:n.599+147A>T
ENST00000469207.5:n.24A>T
ENST00000469550.6:n.1018A>T
ENST00000475549.1:n.276A>T
ENST00000486618.1:n.439A>T
ENST00000491581.5:n.159A>T
ENST00000492407.1:n.767+147A>T
NM_003883.3:c.945A>T	NP_003874.2:p.Val315=
XM_011537697.1:c.384A>T	XP_011535999.1:p.Val128=
XR_944336.1:n.1030A>T
NM_001355039.1:c.945A>T	NP_001341968.1:p.Val315=
NM_001355040.1:c.486A>T	NP_001341969.1:p.Val162=
NM_001355041.1:c.384A>T	NP_001341970.1:p.Val128=
NR_149164.1:n.1011A>T
NR_149165.1:n.893A>T
NR_149166.1:n.843+147A>T
NR_149167.1:n.1011+147A>T
NR_149168.1:n.1036A>T
NR_149169.1:n.1036A>T
NM_003883.4:c.945A>T MANE Select	NP_003874.2:p.Val315=
NM_001355039.2:c.945A>T	NP_001341968.1:p.Val315=
NR_149167.2:n.1004+147A>T
NM_001355040.2:c.486A>T	NP_001341969.1:p.Val162=
NM_001355041.2:c.384A>T	NP_001341970.1:p.Val128=
NR_149164.2:n.1004A>T
NR_149165.2:n.886A>T
NR_149166.2:n.836+147A>T
NR_149168.2:n.1029A>T
NR_149169.2:n.1029A>T