Canonical Allele Identifier: CA398449053

Gene: NCOR1

Linked Data

• COSMIC: COSM1479270 ; COSM4813502
• MyVariant Identifiers: chr17:g.15995175A>G (hg19) ; chr17:g.16091861A>G (hg38)
• MutSpliceDB: CA398449053

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16091861A>G , CM000679.2:g.16091861A>G	GRCh38
NC_000017.10:g.15995175A>G , CM000679.1:g.15995175A>G	GRCh37
NC_000017.9:g.15935900A>G	NCBI36
NG_047111.1:g.129886T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436068.2:c.3064+2T>C	ENSP00000389839.2:n.3064+2T>C
ENST00000704743.1:n.1790+2T>C
ENST00000704744.1:c.3064+2T>C	ENSP00000516021.1:n.3064+2T>C
ENST00000704745.1:c.3094+2T>C	ENSP00000516022.1:n.3094+2T>C
ENST00000268712.8:c.3016+2T>C MANE Select	ENSP00000268712.2:n.3016+2T>C
ENST00000268712.7:c.3016+2T>C	ENSP00000268712.2:n.3016+2T>C
ENST00000395848.5:c.2739T>C	ENSP00000379189.1:p.Gly913=
ENST00000395851.5:c.3064+2T>C	ENSP00000379192.1:n.3064+2T>C
ENST00000395857.7:c.2737+2T>C	ENSP00000379198.4:n.2737+2T>C
ENST00000436068.1:c.56+2T>C
NM_001190438.1:c.2739T>C	NP_001177367.1:p.Gly913=
NM_001190440.1:c.3064+2T>C	NP_001177369.1:n.3064+2T>C
NM_006311.3:c.3016+2T>C	NP_006302.2:n.3016+2T>C
XM_005256866.3:c.3094+2T>C	XP_005256923.1:n.3094+2T>C
XM_005256867.3:c.3094+2T>C	XP_005256924.1:n.3094+2T>C
XM_005256868.3:c.3091+2T>C	XP_005256925.1:n.3091+2T>C
XM_005256871.3:c.3067+2T>C	XP_005256928.1:n.3067+2T>C
XM_005256872.3:c.3064+2T>C	XP_005256929.1:n.3064+2T>C
XM_005256873.3:c.3046+2T>C	XP_005256930.1:n.3046+2T>C
XM_005256874.3:c.3094+2T>C	XP_005256931.1:n.3094+2T>C
XM_005256875.2:c.3094+2T>C	XP_005256932.1:n.3094+2T>C
XM_006721601.2:c.3094+2T>C	XP_006721664.1:n.3094+2T>C
XM_006721602.2:c.3091+2T>C	XP_006721665.1:n.3091+2T>C
XM_006721603.2:c.3094+2T>C	XP_006721666.1:n.3094+2T>C
XM_006721604.2:c.3064+2T>C	XP_006721667.1:n.3064+2T>C
XM_011524083.1:c.3094+2T>C	XP_011522385.1:n.3094+2T>C
XM_011524084.1:c.3094+2T>C	XP_011522386.1:n.3094+2T>C
XM_011524085.1:c.3094+2T>C	XP_011522387.1:n.3094+2T>C
XM_011524086.1:c.3064+2T>C	XP_011522388.1:n.3064+2T>C
XM_005256866.5:c.3094+2T>C	XP_005256923.1:n.3094+2T>C
XM_005256868.5:c.3091+2T>C	XP_005256925.1:n.3091+2T>C
XM_005256871.5:c.3067+2T>C	XP_005256928.1:n.3067+2T>C
XM_005256872.5:c.3064+2T>C	XP_005256929.1:n.3064+2T>C
XM_005256873.5:c.3046+2T>C	XP_005256930.1:n.3046+2T>C
XM_005256874.5:c.3094+2T>C	XP_005256931.1:n.3094+2T>C
XM_005256875.4:c.3094+2T>C	XP_005256932.1:n.3094+2T>C
XM_006721601.4:c.3094+2T>C	XP_006721664.1:n.3094+2T>C
XM_006721602.4:c.3091+2T>C	XP_006721665.1:n.3091+2T>C
XM_006721603.4:c.3094+2T>C	XP_006721666.1:n.3094+2T>C
XM_006721604.4:c.3064+2T>C	XP_006721667.1:n.3064+2T>C
XM_011524083.3:c.3094+2T>C	XP_011522385.1:n.3094+2T>C
XM_011524084.3:c.3094+2T>C	XP_011522386.1:n.3094+2T>C
XM_011524085.3:c.3094+2T>C	XP_011522387.1:n.3094+2T>C
XM_011524086.3:c.3064+2T>C	XP_011522388.1:n.3064+2T>C
XM_017025396.2:c.3094+2T>C	XP_016880885.1:n.3094+2T>C
XM_017025397.2:c.3094+2T>C	XP_016880886.1:n.3094+2T>C
XM_017025398.2:c.3094+2T>C	XP_016880887.1:n.3094+2T>C
XM_017025399.2:c.3094+2T>C	XP_016880888.1:n.3094+2T>C
XM_017025400.2:c.3091+2T>C	XP_016880889.1:n.3091+2T>C
XM_017025401.2:c.3091+2T>C	XP_016880890.1:n.3091+2T>C
XM_017025402.2:c.3091+2T>C	XP_016880891.1:n.3091+2T>C
XM_017025403.2:c.3067+2T>C	XP_016880892.1:n.3067+2T>C
XM_017025404.2:c.3067+2T>C	XP_016880893.1:n.3067+2T>C
XM_017025405.2:c.3067+2T>C	XP_016880894.1:n.3067+2T>C
XM_017025406.2:c.3067+2T>C	XP_016880895.1:n.3067+2T>C
XM_017025407.2:c.3067+2T>C	XP_016880896.1:n.3067+2T>C
XM_017025408.2:c.3067+2T>C	XP_016880897.1:n.3067+2T>C
XM_017025409.2:c.3064+2T>C	XP_016880898.1:n.3064+2T>C
XM_017025410.2:c.3064+2T>C	XP_016880899.1:n.3064+2T>C
XM_017025411.2:c.3064+2T>C	XP_016880900.1:n.3064+2T>C
XM_017025412.2:c.3064+2T>C	XP_016880901.1:n.3064+2T>C
XM_017025413.2:c.3064+2T>C	XP_016880902.1:n.3064+2T>C
XM_017025414.2:c.3064+2T>C	XP_016880903.1:n.3064+2T>C
XM_017025415.2:c.3094+2T>C	XP_016880904.1:n.3094+2T>C
XM_017025416.2:c.3064+2T>C	XP_016880905.1:n.3064+2T>C
XM_017025417.2:c.3046+2T>C	XP_016880906.1:n.3046+2T>C
XM_017025418.2:c.3094+2T>C	XP_016880907.1:n.3094+2T>C
XM_017025419.2:c.3094+2T>C	XP_016880908.1:n.3094+2T>C
XM_017025420.2:c.3046+2T>C	XP_016880909.1:n.3046+2T>C
XM_024451041.1:c.3091+2T>C	XP_024306809.1:n.3091+2T>C
XM_024451042.1:c.3067+2T>C	XP_024306810.1:n.3067+2T>C
XM_024451043.1:c.3064+2T>C	XP_024306811.1:n.3064+2T>C
NM_006311.4:c.3016+2T>C MANE Select	NP_006302.2:n.3016+2T>C