Canonical Allele Identifier: CA10386346
Gene: BCOR HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000378444.9:c.4936dup MANE Select ENSP00000367705.4:p.Leu1646ProfsTer6
ENST00000406200.4:c.4936dup ENSP00000384485.3:p.Leu1646ProfsTer6
ENST00000413905.6:c.4834dup ENSP00000408006.2:p.Leu1612ProfsTer6
ENST00000427012.3:c.4882dup ENSP00000403823.3:p.Leu1628ProfsTer6
ENST00000442018.6:c.4936dup ENSP00000387552.2:p.Leu1646ProfsTer6
ENST00000615339.2:c.4936dup ENSP00000483217.2:p.Leu1646ProfsTer6
ENST00000672265.1:n.1061dup
ENST00000672922.2:c.4936dup ENSP00000499892.2:p.Leu1646ProfsTer6
ENST00000673391.1:c.4834dup ENSP00000500446.1:p.Leu1612ProfsTer6
ENST00000679513.1:c.4936dup ENSP00000505761.1:p.Leu1646ProfsTer6
ENST00000680831.1:c.4936dup ENSP00000505507.1:p.Leu1646ProfsTer6
ENST00000342274.8:c.4834dup ENSP00000345923.4:p.Leu1612ProfsTer6
ENST00000378444.8:c.4936dup ENSP00000367705.4:p.Leu1646ProfsTer6
ENST00000378455.8:c.4780dup ENSP00000367716.4:p.Leu1594ProfsTer6
ENST00000378463.5:c.1465dup ENSP00000367724.1:p.Leu489ProfsTer6
ENST00000397354.7:c.4834dup ENSP00000380512.3:p.Leu1612ProfsTer6
ENST00000413905.5:c.1546dup ENSP00000408006.1:p.Leu516ProfsTer6
ENST00000427012.1:c.825+1442dup
ENST00000442018.5:c.955dup ENSP00000387552.1:p.Leu319ProfsTer6
NM_001123383.1:c.4834dup , LRG_627t1:c.4834dup NP_001116855.1:p.Leu1612ProfsTer6
NM_001123384.1:c.4780dup NP_001116856.1:p.Leu1594ProfsTer6
NM_001123385.1:c.4936dup , LRG_627t2:c.4936dup NP_001116857.1:p.Leu1646ProfsTer6
NM_017745.5:c.4834dup NP_060215.4:p.Leu1612ProfsTer6
XM_005272616.1:c.4936dup XP_005272673.1:p.Leu1646ProfsTer6
XM_005272618.2:c.4936dup XP_005272675.1:p.Leu1646ProfsTer6
XM_005272619.3:c.4882dup XP_005272676.1:p.Leu1628ProfsTer6
XM_005272620.3:c.4780dup XP_005272677.1:p.Leu1594ProfsTer6
XM_006724536.2:c.4936dup XP_006724599.1:p.Leu1646ProfsTer6
XM_011543929.1:c.4936dup XP_011542231.1:p.Leu1646ProfsTer6
XM_011543930.1:c.4936dup XP_011542232.1:p.Leu1646ProfsTer6
XM_011543931.1:c.4936dup XP_011542233.1:p.Leu1646ProfsTer6
XM_005272618.3:c.4936dup XP_005272675.1:p.Leu1646ProfsTer6
XM_005272619.4:c.4882dup XP_005272676.1:p.Leu1628ProfsTer6
XM_005272620.4:c.4780dup XP_005272677.1:p.Leu1594ProfsTer6
XM_006724536.3:c.4936dup XP_006724599.1:p.Leu1646ProfsTer6
XM_011543929.2:c.4936dup XP_011542231.1:p.Leu1646ProfsTer6
XM_011543931.2:c.4936dup XP_011542233.1:p.Leu1646ProfsTer6
XM_017029615.1:c.4834dup XP_016885104.1:p.Leu1612ProfsTer6
XM_017029616.2:c.4936dup XP_016885105.1:p.Leu1646ProfsTer6
NM_001123384.2:c.4780dup NP_001116856.1:p.Leu1594ProfsTer6
NM_001123385.2:c.4936dup MANE Select NP_001116857.1:p.Leu1646ProfsTer6
NM_017745.6:c.4834dup NP_060215.4:p.Leu1612ProfsTer6