Canonical Allele Identifier: CA361515035

Gene: HDAC3

Linked Data

• gnomAD v4: 5-141626022-G-A
• MyVariant Identifiers: chr5:g.141005589G>A (hg19) ; chr5:g.141626022G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626022G>A , CM000667.2:g.141626022G>A	GRCh38
NC_000005.9:g.141005589G>A , CM000667.1:g.141005589G>A	GRCh37
NC_000005.8:g.140985773G>A	NCBI36
NG_029678.1:g.15835C>T
NG_029678.2:g.15835C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.970C>T MANE Select	ENSP00000302967.3:p.Pro324Ser
ENST00000305264.7:c.970C>T	ENSP00000302967.3:p.Pro324Ser
ENST00000459727.5:n.233+172C>T
ENST00000467533.5:n.599+172C>T
ENST00000469207.5:n.49C>T
ENST00000469550.6:n.1043C>T
ENST00000486618.1:n.464C>T
ENST00000491581.5:n.184C>T
ENST00000492407.1:n.767+172C>T
NM_003883.3:c.970C>T	NP_003874.2:p.Pro324Ser
XM_011537697.1:c.409C>T	XP_011535999.1:p.Pro137Ser
XR_944336.1:n.1055C>T
NM_001355039.1:c.970C>T	NP_001341968.1:p.Pro324Ser
NM_001355040.1:c.511C>T	NP_001341969.1:p.Pro171Ser
NM_001355041.1:c.409C>T	NP_001341970.1:p.Pro137Ser
NR_149164.1:n.1036C>T
NR_149165.1:n.918C>T
NR_149166.1:n.843+172C>T
NR_149167.1:n.1011+172C>T
NR_149168.1:n.1061C>T
NR_149169.1:n.1061C>T
NM_003883.4:c.970C>T MANE Select	NP_003874.2:p.Pro324Ser
NM_001355039.2:c.970C>T	NP_001341968.1:p.Pro324Ser
NR_149167.2:n.1004+172C>T
NM_001355040.2:c.511C>T	NP_001341969.1:p.Pro171Ser
NM_001355041.2:c.409C>T	NP_001341970.1:p.Pro137Ser
NR_149164.2:n.1029C>T
NR_149165.2:n.911C>T
NR_149166.2:n.836+172C>T
NR_149168.2:n.1054C>T
NR_149169.2:n.1054C>T