Canonical Allele Identifier: CA8408115

Gene: NCOR1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16057910G>T , CM000679.2:g.16057910G>T	GRCh38
NC_000017.10:g.15961224G>T , CM000679.1:g.15961224G>T	GRCh37
NC_000017.9:g.15901949G>T	NCBI36
NG_047111.1:g.163837C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.6387C>A	ENSP00000389839.2:p.Ile2129=
ENST00000704743.1:n.5113C>A
ENST00000704744.1:c.6387C>A	ENSP00000516021.1:p.Ile2129=
ENST00000704745.1:c.6243C>A	ENSP00000516022.1:p.Ile2081=
ENST00000268712.8:c.6165C>A MANE Select	ENSP00000268712.2:p.Ile2055=
ENST00000268712.7:c.6165C>A	ENSP00000268712.2:p.Ile2055=
ENST00000395849.6:c.2057C>A
ENST00000395851.5:c.5856C>A	ENSP00000379192.1:p.Ile1952=
ENST00000395857.7:c.5877C>A	ENSP00000379198.4:p.Ile1959=
ENST00000458113.6:n.2925C>A
ENST00000464381.5:n.427C>A
ENST00000470782.5:n.1940C>A
ENST00000472189.1:n.26C>A
NM_001190440.1:c.5856C>A	NP_001177369.1:p.Ile1952=
NM_006311.3:c.6165C>A	NP_006302.2:p.Ile2055=
XM_005256866.3:c.6417C>A	XP_005256923.1:p.Ile2139=
XM_005256867.3:c.6417C>A	XP_005256924.1:p.Ile2139=
XM_005256868.3:c.6414C>A	XP_005256925.1:p.Ile2138=
XM_005256871.3:c.6390C>A	XP_005256928.1:p.Ile2130=
XM_005256872.3:c.6387C>A	XP_005256929.1:p.Ile2129=
XM_005256873.3:c.6369C>A	XP_005256930.1:p.Ile2123=
XM_005256874.3:c.6243C>A	XP_005256931.1:p.Ile2081=
XM_005256875.2:c.6189C>A	XP_005256932.1:p.Ile2063=
XM_006721601.2:c.6417C>A	XP_006721664.1:p.Ile2139=
XM_006721602.2:c.6414C>A	XP_006721665.1:p.Ile2138=
XM_006721603.2:c.6417C>A	XP_006721666.1:p.Ile2139=
XM_006721604.2:c.6213C>A	XP_006721667.1:p.Ile2071=
XM_011524083.1:c.6417C>A	XP_011522385.1:p.Ile2139=
XM_011524084.1:c.6417C>A	XP_011522386.1:p.Ile2139=
XM_011524085.1:c.6060C>A	XP_011522387.1:p.Ile2020=
XM_011524086.1:c.5856C>A	XP_011522388.1:p.Ile1952=
XM_005256866.5:c.6417C>A	XP_005256923.1:p.Ile2139=
XM_005256868.5:c.6414C>A	XP_005256925.1:p.Ile2138=
XM_005256871.5:c.6390C>A	XP_005256928.1:p.Ile2130=
XM_005256872.5:c.6387C>A	XP_005256929.1:p.Ile2129=
XM_005256873.5:c.6369C>A	XP_005256930.1:p.Ile2123=
XM_005256874.5:c.6243C>A	XP_005256931.1:p.Ile2081=
XM_005256875.4:c.6189C>A	XP_005256932.1:p.Ile2063=
XM_006721601.4:c.6417C>A	XP_006721664.1:p.Ile2139=
XM_006721602.4:c.6414C>A	XP_006721665.1:p.Ile2138=
XM_006721603.4:c.6417C>A	XP_006721666.1:p.Ile2139=
XM_006721604.4:c.6213C>A	XP_006721667.1:p.Ile2071=
XM_011524083.3:c.6417C>A	XP_011522385.1:p.Ile2139=
XM_011524084.3:c.6417C>A	XP_011522386.1:p.Ile2139=
XM_011524085.3:c.6060C>A	XP_011522387.1:p.Ile2020=
XM_011524086.3:c.5856C>A	XP_011522388.1:p.Ile1952=
XM_017025396.2:c.6417C>A	XP_016880885.1:p.Ile2139=
XM_017025397.2:c.6417C>A	XP_016880886.1:p.Ile2139=
XM_017025398.2:c.6417C>A	XP_016880887.1:p.Ile2139=
XM_017025399.2:c.6417C>A	XP_016880888.1:p.Ile2139=
XM_017025400.2:c.6414C>A	XP_016880889.1:p.Ile2138=
XM_017025401.2:c.6414C>A	XP_016880890.1:p.Ile2138=
XM_017025402.2:c.6414C>A	XP_016880891.1:p.Ile2138=
XM_017025403.2:c.6390C>A	XP_016880892.1:p.Ile2130=
XM_017025404.2:c.6390C>A	XP_016880893.1:p.Ile2130=
XM_017025405.2:c.6390C>A	XP_016880894.1:p.Ile2130=
XM_017025406.2:c.6390C>A	XP_016880895.1:p.Ile2130=
XM_017025407.2:c.6390C>A	XP_016880896.1:p.Ile2130=
XM_017025408.2:c.6390C>A	XP_016880897.1:p.Ile2130=
XM_017025409.2:c.6387C>A	XP_016880898.1:p.Ile2129=
XM_017025410.2:c.6387C>A	XP_016880899.1:p.Ile2129=
XM_017025411.2:c.6387C>A	XP_016880900.1:p.Ile2129=
XM_017025412.2:c.6387C>A	XP_016880901.1:p.Ile2129=
XM_017025413.2:c.6387C>A	XP_016880902.1:p.Ile2129=
XM_017025414.2:c.6387C>A	XP_016880903.1:p.Ile2129=
XM_017025415.2:c.6243C>A	XP_016880904.1:p.Ile2081=
XM_017025416.2:c.6213C>A	XP_016880905.1:p.Ile2071=
XM_017025417.2:c.6195C>A	XP_016880906.1:p.Ile2065=
XM_017025418.2:c.6060C>A	XP_016880907.1:p.Ile2020=
XM_017025419.2:c.5886C>A	XP_016880908.1:p.Ile1962=
XM_017025420.2:c.5838C>A	XP_016880909.1:p.Ile1946=
XM_024451041.1:c.6414C>A	XP_024306809.1:p.Ile2138=
XM_024451042.1:c.6390C>A	XP_024306810.1:p.Ile2130=
XM_024451043.1:c.6387C>A	XP_024306811.1:p.Ile2129=
NM_006311.4:c.6165C>A MANE Select	NP_006302.2:p.Ile2055=