Canonical Allele Identifier: CA2069256269

Gene: NCOR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124390966C= , CM000674.2:g.124390966C=	GRCh38
NC_000012.11:g.124875512C= , CM000674.1:g.124875512C=	GRCh37
NC_000012.10:g.123441465C=	NCBI36
NG_022928.2:g.181499G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000405201.6:c.1877-5079G= MANE Select	ENSP00000384018.1:n.1877-5079G=
ENST00000356219.7:c.548-5079G=	ENSP00000348551.4:n.548-5079G=
ENST00000404121.6:c.548-5079G=	ENSP00000385618.3:n.548-5079G=
ENST00000404621.5:c.1874-5079G=	ENSP00000384202.1:n.1874-5079G=
ENST00000405201.5:c.1877-5079G=	ENSP00000384018.1:n.1877-5079G=
ENST00000429285.6:c.1874-5079G=	ENSP00000400281.2:n.1874-5079G=
ENST00000458234.5:c.1877-5079G=	ENSP00000402808.1:n.1877-5079G=
NM_001077261.3:c.1874-5079G=	NP_001070729.2:n.1874-5079G=
NM_001206654.1:c.1874-5079G=	NP_001193583.1:n.1874-5079G=
NM_006312.5:c.1877-5079G=	NP_006303.4:n.1877-5079G=
NM_001077261.4:c.1874-5079G=	NP_001070729.2:n.1874-5079G=
NM_001206654.2:c.1874-5079G=	NP_001193583.1:n.1874-5079G=
NM_006312.6:c.1877-5079G= MANE Select	NP_006303.4:n.1877-5079G=