Canonical Allele Identifier: CA15429270

Gene: HDAC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.113964089C>T , CM000668.2:g.113964089C>T	GRCh38
NC_000006.11:g.114285253C>T , CM000668.1:g.114285253C>T	GRCh37
NC_000006.10:g.114391946C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519065.6:c.53-4071G>A MANE Select	ENSP00000430432.1:n.53-4071G>A
ENST00000368632.6:c.-66-1695G>A	ENSP00000357621.2:n.-66-1695G>A
ENST00000425835.6:c.23-4071G>A	ENSP00000417026.2:n.23-4071G>A
ENST00000518690.5:c.-38-4071G>A	ENSP00000428653.1:n.-38-4071G>A
ENST00000519065.5:c.53-4071G>A	ENSP00000430432.1:n.53-4071G>A
ENST00000519108.5:c.-38-4071G>A	ENSP00000430008.1:n.-38-4071G>A
ENST00000520170.1:n.282-4071G>A
ENST00000520895.5:c.-38-4071G>A	ENSP00000428861.1:n.-38-4071G>A
ENST00000521163.5:c.53-4050G>A	ENSP00000428024.1:n.53-4050G>A
ENST00000521233.1:n.281-4071G>A
ENST00000521610.5:c.-38-4071G>A	ENSP00000429901.1:n.-38-4071G>A
ENST00000522371.5:c.-66-1695G>A	ENSP00000428599.1:n.-66-1695G>A
ENST00000523240.5:c.-66-1695G>A	ENSP00000429236.1:n.-66-1695G>A
ENST00000523628.5:c.-38-4071G>A	ENSP00000427861.1:n.-38-4071G>A
ENST00000524334.1:c.-66-1695G>A	ENSP00000428989.1:n.-66-1695G>A
NM_001527.3:c.53-4071G>A	NP_001518.3:n.53-4071G>A
NR_033441.1:n.340-1695G>A
NR_073443.1:n.246-4071G>A
XM_011535786.1:c.53-4071G>A	XP_011534088.1:n.53-4071G>A
XM_011535787.1:c.-66-1695G>A	XP_011534089.1:n.-66-1695G>A
XM_011535788.1:c.-66-1695G>A	XP_011534090.1:n.-66-1695G>A
XM_017010799.1:c.-38-4071G>A	XP_016866288.1:n.-38-4071G>A
NM_001527.4:c.53-4071G>A MANE Select	NP_001518.3:n.53-4071G>A
NR_033441.2:n.293-1695G>A
NR_073443.2:n.251-4071G>A