Canonical Allele Identifier: CA1139770881

Gene: BCOR

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.40053931del , CM000685.2:g.40053931del	GRCh38
NC_000023.10:g.39913184del , CM000685.1:g.39913184del	GRCh37
NC_000023.9:g.39798128del	NCBI36
NG_008880.1:g.128404del , LRG_627:g.128404del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378444.9:c.4936del MANE Select	ENSP00000367705.4:p.Leu1646SerfsTer28
ENST00000406200.4:c.4936del	ENSP00000384485.3:p.Leu1646SerfsTer28
ENST00000413905.6:c.4834del	ENSP00000408006.2:p.Leu1612SerfsTer28
ENST00000427012.3:c.4882del	ENSP00000403823.3:p.Leu1628SerfsTer28
ENST00000442018.6:c.4936del	ENSP00000387552.2:p.Leu1646SerfsTer24
ENST00000615339.2:c.4936del	ENSP00000483217.2:p.Leu1646SerfsTer28
ENST00000672265.1:n.1061del
ENST00000672922.2:c.4936del	ENSP00000499892.2:p.Leu1646SerfsTer28
ENST00000673391.1:c.4834del	ENSP00000500446.1:p.Leu1612SerfsTer28
ENST00000679513.1:c.4936del	ENSP00000505761.1:p.Leu1646SerfsTer28
ENST00000680831.1:c.4936del	ENSP00000505507.1:p.Leu1646SerfsTer28
ENST00000342274.8:c.4834del	ENSP00000345923.4:p.Leu1612SerfsTer28
ENST00000378444.8:c.4936del	ENSP00000367705.4:p.Leu1646SerfsTer28
ENST00000378455.8:c.4780del	ENSP00000367716.4:p.Leu1594SerfsTer28
ENST00000378463.5:c.1465del	ENSP00000367724.1:p.Leu489SerfsTer28
ENST00000397354.7:c.4834del	ENSP00000380512.3:p.Leu1612SerfsTer28
ENST00000413905.5:c.1546del	ENSP00000408006.1:p.Leu516SerfsTer28
ENST00000427012.1:c.825+1442del
ENST00000442018.5:c.955del	ENSP00000387552.1:p.Leu319SerfsTer24
NM_001123383.1:c.4834del , LRG_627t1:c.4834del	NP_001116855.1:p.Leu1612SerfsTer28
NM_001123384.1:c.4780del	NP_001116856.1:p.Leu1594SerfsTer28
NM_001123385.1:c.4936del , LRG_627t2:c.4936del	NP_001116857.1:p.Leu1646SerfsTer28
NM_017745.5:c.4834del	NP_060215.4:p.Leu1612SerfsTer28
XM_005272616.1:c.4936del	XP_005272673.1:p.Leu1646SerfsTer28
XM_005272618.2:c.4936del	XP_005272675.1:p.Leu1646SerfsTer28
XM_005272619.3:c.4882del	XP_005272676.1:p.Leu1628SerfsTer28
XM_005272620.3:c.4780del	XP_005272677.1:p.Leu1594SerfsTer28
XM_006724536.2:c.4936del	XP_006724599.1:p.Leu1646SerfsTer28
XM_011543929.1:c.4936del	XP_011542231.1:p.Leu1646SerfsTer28
XM_011543930.1:c.4936del	XP_011542232.1:p.Leu1646SerfsTer28
XM_011543931.1:c.4936del	XP_011542233.1:p.Leu1646SerfsTer28
XM_005272618.3:c.4936del	XP_005272675.1:p.Leu1646SerfsTer28
XM_005272619.4:c.4882del	XP_005272676.1:p.Leu1628SerfsTer28
XM_005272620.4:c.4780del	XP_005272677.1:p.Leu1594SerfsTer28
XM_006724536.3:c.4936del	XP_006724599.1:p.Leu1646SerfsTer28
XM_011543929.2:c.4936del	XP_011542231.1:p.Leu1646SerfsTer28
XM_011543931.2:c.4936del	XP_011542233.1:p.Leu1646SerfsTer28
XM_017029615.1:c.4834del	XP_016885104.1:p.Leu1612SerfsTer28
XM_017029616.2:c.4936del	XP_016885105.1:p.Leu1646SerfsTer24
NM_001123384.2:c.4780del	NP_001116856.1:p.Leu1594SerfsTer28
NM_001123385.2:c.4936del MANE Select	NP_001116857.1:p.Leu1646SerfsTer28
NM_017745.6:c.4834del	NP_060215.4:p.Leu1612SerfsTer28