Canonical Allele Identifier: CA2580100878

Gene: BCOR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.40052402_40052404delinsCAA , CM000685.2:g.40052402_40052404delinsCAA	GRCh38
NC_000023.10:g.39911655_39911657delinsCAA , CM000685.1:g.39911655_39911657delinsCAA	GRCh37
NC_000023.9:g.39796599_39796601delinsCAA	NCBI36
NG_008880.1:g.129926_129928delinsTTG , LRG_627:g.129926_129928delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
NM_001123385.2:c.4977-4_4977-2delinsTTG MANE Select	NP_001116857.1:n.4977-4_4977-2delinsTTG
ENST00000378444.9:c.4977-4_4977-2delinsTTG MANE Select	ENSP00000367705.4:n.4977-4_4977-2delinsTTG
NM_001123383.1:c.4875-4_4875-2delinsTTG , LRG_627t1:c.4875-4_4875-2delinsTTG	NP_001116855.1:n.4875-4_4875-2delinsTTG
NM_001123384.1:c.4821-4_4821-2delinsTTG	NP_001116856.1:n.4821-4_4821-2delinsTTG
NM_001123384.2:c.4821-4_4821-2delinsTTG	NP_001116856.1:n.4821-4_4821-2delinsTTG
NM_001123385.1:c.4977-4_4977-2delinsTTG , LRG_627t2:c.4977-4_4977-2delinsTTG	NP_001116857.1:n.4977-4_4977-2delinsTTG
NM_017745.5:c.4875-4_4875-2delinsTTG	NP_060215.4:n.4875-4_4875-2delinsTTG
NM_017745.6:c.4875-4_4875-2delinsTTG	NP_060215.4:n.4875-4_4875-2delinsTTG
ENST00000342274.8:c.4875-4_4875-2delinsTTG	ENSP00000345923.4:n.4875-4_4875-2delinsTTG
ENST00000378444.8:c.4977-4_4977-2delinsTTG	ENSP00000367705.4:n.4977-4_4977-2delinsTTG
ENST00000378455.8:c.4821-4_4821-2delinsTTG	ENSP00000367716.4:n.4821-4_4821-2delinsTTG
ENST00000378463.5:c.1506-4_1506-2delinsTTG	ENSP00000367724.1:n.1506-4_1506-2delinsTTG
ENST00000397354.7:c.4875-4_4875-2delinsTTG	ENSP00000380512.3:n.4875-4_4875-2delinsTTG
ENST00000406200.4:c.4977-4_4977-2delinsTTG	ENSP00000384485.3:n.4977-4_4977-2delinsTTG
ENST00000413905.5:c.1587-4_1587-2delinsTTG	ENSP00000408006.1:n.1587-4_1587-2delinsTTG
ENST00000413905.6:c.4875-4_4875-2delinsTTG	ENSP00000408006.2:n.4875-4_4875-2delinsTTG
ENST00000427012.1:c.826-4_826-2delinsTTG
ENST00000427012.3:c.4923-4_4923-2delinsTTG	ENSP00000403823.3:n.4923-4_4923-2delinsTTG
ENST00000442018.5:c.1044-4_1044-2delinsTTG	ENSP00000387552.1:n.1044-4_1044-2delinsTTG
ENST00000442018.6:c.5025-4_5025-2delinsTTG	ENSP00000387552.2:n.5025-4_5025-2delinsTTG
ENST00000615339.2:c.4977-4_4977-2delinsTTG	ENSP00000483217.2:n.4977-4_4977-2delinsTTG
ENST00000672265.1:n.1102-4_1102-2delinsTTG
ENST00000672922.2:c.4977-4_4977-2delinsTTG	ENSP00000499892.2:n.4977-4_4977-2delinsTTG
ENST00000673391.1:c.4875-4_4875-2delinsTTG	ENSP00000500446.1:n.4875-4_4875-2delinsTTG
ENST00000679513.1:c.4977-4_4977-2delinsTTG	ENSP00000505761.1:n.4977-4_4977-2delinsTTG
ENST00000680831.1:c.4977-4_4977-2delinsTTG	ENSP00000505507.1:n.4977-4_4977-2delinsTTG
XM_005272616.1:c.4977-4_4977-2delinsTTG	XP_005272673.1:n.4977-4_4977-2delinsTTG
XM_005272618.2:c.4977-4_4977-2delinsTTG	XP_005272675.1:n.4977-4_4977-2delinsTTG
XM_005272618.3:c.4977-4_4977-2delinsTTG	XP_005272675.1:n.4977-4_4977-2delinsTTG
XM_005272619.3:c.4923-4_4923-2delinsTTG	XP_005272676.1:n.4923-4_4923-2delinsTTG
XM_005272619.4:c.4923-4_4923-2delinsTTG	XP_005272676.1:n.4923-4_4923-2delinsTTG
XM_005272620.3:c.4821-4_4821-2delinsTTG	XP_005272677.1:n.4821-4_4821-2delinsTTG
XM_005272620.4:c.4821-4_4821-2delinsTTG	XP_005272677.1:n.4821-4_4821-2delinsTTG
XM_006724536.2:c.4977-4_4977-2delinsTTG	XP_006724599.1:n.4977-4_4977-2delinsTTG
XM_006724536.3:c.4977-4_4977-2delinsTTG	XP_006724599.1:n.4977-4_4977-2delinsTTG
XM_011543929.1:c.4977-4_4977-2delinsTTG	XP_011542231.1:n.4977-4_4977-2delinsTTG
XM_011543929.2:c.4977-4_4977-2delinsTTG	XP_011542231.1:n.4977-4_4977-2delinsTTG
XM_011543930.1:c.4977-4_4977-2delinsTTG	XP_011542232.1:n.4977-4_4977-2delinsTTG
XM_011543931.1:c.4977-4_4977-2delinsTTG	XP_011542233.1:n.4977-4_4977-2delinsTTG
XM_011543931.2:c.4977-4_4977-2delinsTTG	XP_011542233.1:n.4977-4_4977-2delinsTTG
XM_017029615.1:c.4875-4_4875-2delinsTTG	XP_016885104.1:n.4875-4_4875-2delinsTTG
XM_017029616.2:c.*45-4_*45-2delinsTTG	XP_016885105.1:n.*45-4_*45-2delinsTTG