Canonical Allele Identifier: CA255609
Gene: BCOR HGNC NCBI

Linked Data

ClinVar Variation Id: 10913
ClinVar RCV Id: RCV000011660
dbSNP Id: rs121434619

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.40072420G>A , CM000685.2:g.40072420G>A GRCh38
NC_000023.10:g.39931673G>A , CM000685.1:g.39931673G>A GRCh37
NC_000023.9:g.39816617G>A NCBI36
NG_008880.1:g.109910C>T , LRG_627:g.109910C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378444.9:c.2926C>T MANE Select ENSP00000367705.4:p.Arg976Ter
ENST00000406200.4:c.2926C>T ENSP00000384485.3:p.Arg976Ter
ENST00000413905.6:c.2926C>T ENSP00000408006.2:p.Arg976Ter
ENST00000427012.3:c.2926C>T ENSP00000403823.3:p.Arg976Ter
ENST00000442018.6:c.2926C>T ENSP00000387552.2:p.Arg976Ter
ENST00000615339.2:c.2926C>T ENSP00000483217.2:p.Arg976Ter
ENST00000672922.2:c.2926C>T ENSP00000499892.2:p.Arg976Ter
ENST00000673391.1:c.2926C>T ENSP00000500446.1:p.Arg976Ter
ENST00000679513.1:c.2926C>T ENSP00000505761.1:p.Arg976Ter
ENST00000680831.1:c.2926C>T ENSP00000505507.1:p.Arg976Ter
ENST00000342274.8:c.2926C>T ENSP00000345923.4:p.Arg976Ter
ENST00000378444.8:c.2926C>T ENSP00000367705.4:p.Arg976Ter
ENST00000378455.8:c.2926C>T ENSP00000367716.4:p.Arg976Ter
ENST00000397354.7:c.2926C>T ENSP00000380512.3:p.Arg976Ter
ENST00000406200.2:c.2926C>T ENSP00000384485.2:p.Arg976Ter
ENST00000490976.5:n.2966C>T
ENST00000615339.1:c.1147C>T ENSP00000483217.1:p.Arg383Ter
NM_001123383.1:c.2926C>T , LRG_627t1:c.2926C>T NP_001116855.1:p.Arg976Ter
NM_001123384.1:c.2926C>T NP_001116856.1:p.Arg976Ter
NM_001123385.1:c.2926C>T , LRG_627t2:c.2926C>T NP_001116857.1:p.Arg976Ter
NM_017745.5:c.2926C>T NP_060215.4:p.Arg976Ter
XM_005272616.1:c.2926C>T XP_005272673.1:p.Arg976Ter
XM_005272618.2:c.2926C>T XP_005272675.1:p.Arg976Ter
XM_005272619.3:c.2926C>T XP_005272676.1:p.Arg976Ter
XM_005272620.3:c.2926C>T XP_005272677.1:p.Arg976Ter
XM_006724536.2:c.2926C>T XP_006724599.1:p.Arg976Ter
XM_011543929.1:c.2926C>T XP_011542231.1:p.Arg976Ter
XM_011543930.1:c.2926C>T XP_011542232.1:p.Arg976Ter
XM_011543931.1:c.2926C>T XP_011542233.1:p.Arg976Ter
XM_005272618.3:c.2926C>T XP_005272675.1:p.Arg976Ter
XM_005272619.4:c.2926C>T XP_005272676.1:p.Arg976Ter
XM_005272620.4:c.2926C>T XP_005272677.1:p.Arg976Ter
XM_006724536.3:c.2926C>T XP_006724599.1:p.Arg976Ter
XM_011543929.2:c.2926C>T XP_011542231.1:p.Arg976Ter
XM_011543931.2:c.2926C>T XP_011542233.1:p.Arg976Ter
XM_017029615.1:c.2926C>T XP_016885104.1:p.Arg976Ter
XM_017029616.2:c.2926C>T XP_016885105.1:p.Arg976Ter
NM_001123384.2:c.2926C>T NP_001116856.1:p.Arg976Ter
NM_001123385.2:c.2926C>T MANE Select NP_001116857.1:p.Arg976Ter
NM_017745.6:c.2926C>T NP_060215.4:p.Arg976Ter