Canonical Allele Identifier: CA2664547424

Gene: HDAC11

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.13504027C>G , CM000665.2:g.13504027C>G	GRCh38
NC_000003.11:g.13545527C>G , CM000665.1:g.13545527C>G	GRCh37
NC_000003.10:g.13520527C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024827.4:c.650-67C>G MANE Select	NP_079103.2:n.650-67C>G
ENST00000295757.8:c.650-67C>G MANE Select	ENSP00000295757.3:n.650-67C>G
NM_001136041.2:c.497-67C>G	NP_001129513.1:n.497-67C>G
NM_001136041.3:c.497-67C>G	NP_001129513.1:n.497-67C>G
NM_001330636.1:c.413-67C>G	NP_001317565.1:n.413-67C>G
NM_001330636.2:c.413-67C>G	NP_001317565.1:n.413-67C>G
NM_024827.3:c.650-67C>G	NP_079103.2:n.650-67C>G
ENST00000295757.7:c.650-67C>G	ENSP00000295757.3:n.650-67C>G
ENST00000402259.5:c.152-67C>G	ENSP00000384706.1:n.152-67C>G
ENST00000402271.5:c.413-67C>G	ENSP00000384123.1:n.413-67C>G
ENST00000404040.5:c.350-67C>G	ENSP00000385475.1:n.350-67C>G
ENST00000404548.5:c.253-67C>G	ENSP00000385528.1:n.253-67C>G
ENST00000405025.5:c.169-67C>G	ENSP00000384019.1:n.169-67C>G
ENST00000405478.5:c.566-67C>G	ENSP00000385252.1:n.566-67C>G
ENST00000425430.5:c.*150-67C>G	ENSP00000399792.1:n.*150-67C>G
ENST00000433119.5:c.523-67C>G	ENSP00000412514.1:n.523-67C>G
ENST00000437379.2:c.566-67C>G	ENSP00000395188.2:n.566-67C>G
ENST00000446613.6:c.523-67C>G	ENSP00000401487.3:n.523-67C>G
ENST00000498532.5:n.546-67C>G
ENST00000522202.5:c.497-67C>G	ENSP00000429794.1:n.497-67C>G
XM_005265491.1:c.566-67C>G	XP_005265548.1:n.566-67C>G
XM_005265492.1:c.413-67C>G	XP_005265549.1:n.413-67C>G
XM_005265493.1:c.490-67C>G	XP_005265550.1:n.490-67C>G
XM_006713338.1:c.413-67C>G	XP_006713401.1:n.413-67C>G
XM_011534130.1:c.707-67C>G	XP_011532432.1:n.707-67C>G
XM_011534131.1:c.566-67C>G	XP_011532433.1:n.566-67C>G
XM_011534132.1:c.470-67C>G	XP_011532434.1:n.470-67C>G
XM_011534132.2:c.329-67C>G	XP_011532434.2:n.329-67C>G
XM_011534133.1:c.470-67C>G	XP_011532435.1:n.470-67C>G
XM_011534134.1:c.547-67C>G	XP_011532436.1:n.547-67C>G
XM_011534135.1:c.284-67C>G	XP_011532437.1:n.284-67C>G
XM_017007234.1:c.329-67C>G	XP_016862723.1:n.329-67C>G
XM_024453761.1:c.566-67C>G	XP_024309529.1:n.566-67C>G
XM_024453762.1:c.470-67C>G	XP_024309530.1:n.470-67C>G
XM_024453763.1:c.547-67C>G	XP_024309531.1:n.547-67C>G
XM_024453764.1:c.329-67C>G	XP_024309532.1:n.329-67C>G
XM_024453765.1:c.329-67C>G	XP_024309533.1:n.329-67C>G