Canonical Allele Identifier: CA245215715

Gene: NCOR2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124409638T>G , CM000674.2:g.124409638T>G	GRCh38
NC_000012.11:g.124894184T>G , CM000674.1:g.124894184T>G	GRCh37
NC_000012.10:g.123460137T>G	NCBI36
NG_022928.2:g.162827A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405201.6:c.1483-7077A>C MANE Select	ENSP00000384018.1:n.1483-7077A>C
ENST00000356219.7:c.154-7077A>C	ENSP00000348551.4:n.154-7077A>C
ENST00000404121.6:c.154-7077A>C	ENSP00000385618.3:n.154-7077A>C
ENST00000404621.5:c.1480-7077A>C	ENSP00000384202.1:n.1480-7077A>C
ENST00000405201.5:c.1483-7077A>C	ENSP00000384018.1:n.1483-7077A>C
ENST00000429285.6:c.1480-7077A>C	ENSP00000400281.2:n.1480-7077A>C
ENST00000458234.5:c.1483-7077A>C	ENSP00000402808.1:n.1483-7077A>C
NM_001077261.3:c.1480-7077A>C	NP_001070729.2:n.1480-7077A>C
NM_001206654.1:c.1480-7077A>C	NP_001193583.1:n.1480-7077A>C
NM_006312.5:c.1483-7077A>C	NP_006303.4:n.1483-7077A>C
NM_001077261.4:c.1480-7077A>C	NP_001070729.2:n.1480-7077A>C
NM_001206654.2:c.1480-7077A>C	NP_001193583.1:n.1480-7077A>C
NM_006312.6:c.1483-7077A>C MANE Select	NP_006303.4:n.1483-7077A>C