Canonical Allele Identifier: CA2069281561

Gene: NCOR2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124341916C= , CM000674.2:g.124341916C=	GRCh38
NC_000012.11:g.124826462C= , CM000674.1:g.124826462C=	GRCh37
NC_000012.10:g.123392415C=	NCBI36
NG_022928.2:g.230549G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.5095G= MANE Select	ENSP00000384018.1:p.Ala1699=
ENST00000356219.7:c.3790G=	ENSP00000348551.4:p.Ala1264=
ENST00000404121.6:c.3739G=	ENSP00000385618.3:p.Ala1247=
ENST00000404621.5:c.5065G=	ENSP00000384202.1:p.Ala1689=
ENST00000405201.5:c.5095G=	ENSP00000384018.1:p.Ala1699=
ENST00000429285.6:c.5065G=	ENSP00000400281.2:p.Ala1689=
ENST00000453428.1:c.140G=
NM_001077261.3:c.5065G=	NP_001070729.2:p.Ala1689=
NM_001206654.1:c.5065G=	NP_001193583.1:p.Ala1689=
NM_006312.5:c.5095G=	NP_006303.4:p.Ala1699=
NM_001077261.4:c.5065G=	NP_001070729.2:p.Ala1689=
NM_001206654.2:c.5065G=	NP_001193583.1:p.Ala1689=
NM_006312.6:c.5095G= MANE Select	NP_006303.4:p.Ala1699=