Canonical Allele Identifier: CA361515532

Gene: HDAC3

Linked Data

• MyVariant Identifiers: chr5:g.141005633T>G (hg19) ; chr5:g.141626066T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.141626066T>G , CM000667.2:g.141626066T>G	GRCh38
NC_000005.9:g.141005633T>G , CM000667.1:g.141005633T>G	GRCh37
NC_000005.8:g.140985817T>G	NCBI36
NG_029678.1:g.15791A>C
NG_029678.2:g.15791A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000305264.8:c.926A>C MANE Select	ENSP00000302967.3:p.Tyr309Ser
ENST00000305264.7:c.926A>C	ENSP00000302967.3:p.Tyr309Ser
ENST00000459727.5:n.233+128A>C
ENST00000467533.5:n.599+128A>C
ENST00000469207.5:n.5A>C
ENST00000469550.6:n.999A>C
ENST00000475549.1:n.257A>C
ENST00000486618.1:n.420A>C
ENST00000491581.5:n.140A>C
ENST00000492407.1:n.767+128A>C
NM_003883.3:c.926A>C	NP_003874.2:p.Tyr309Ser
XM_011537697.1:c.365A>C	XP_011535999.1:p.Tyr122Ser
XR_944336.1:n.1011A>C
NM_001355039.1:c.926A>C	NP_001341968.1:p.Tyr309Ser
NM_001355040.1:c.467A>C	NP_001341969.1:p.Tyr156Ser
NM_001355041.1:c.365A>C	NP_001341970.1:p.Tyr122Ser
NR_149164.1:n.992A>C
NR_149165.1:n.874A>C
NR_149166.1:n.843+128A>C
NR_149167.1:n.1011+128A>C
NR_149168.1:n.1017A>C
NR_149169.1:n.1017A>C
NM_003883.4:c.926A>C MANE Select	NP_003874.2:p.Tyr309Ser
NM_001355039.2:c.926A>C	NP_001341968.1:p.Tyr309Ser
NR_149167.2:n.1004+128A>C
NM_001355040.2:c.467A>C	NP_001341969.1:p.Tyr156Ser
NM_001355041.2:c.365A>C	NP_001341970.1:p.Tyr122Ser
NR_149164.2:n.985A>C
NR_149165.2:n.867A>C
NR_149166.2:n.836+128A>C
NR_149168.2:n.1010A>C
NR_149169.2:n.1010A>C