Canonical Allele Identifier: CA157323

Gene: BCOR

Linked Data

• ClinVar Variation Id: 133685
• ClinVar RCV Id: RCV000120213 ; RCV000861482
• dbSNP Id: rs143697110
• ExAC: X:39933973 G / A
• gnomAD v2: X-39933973-G-A
• gnomAD v3: X-40074720-G-A
• gnomAD v4: X-40074720-G-A
• COSMIC: COSM6023039
• MyVariant Identifiers: chrX:g.39933973G>A (hg19) ; chrX:g.40074720G>A (hg38)
• PubMed: PMID:24728327

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.40074720G>A , CM000685.2:g.40074720G>A	GRCh38
NC_000023.10:g.39933973G>A , CM000685.1:g.39933973G>A	GRCh37
NC_000023.9:g.39818917G>A	NCBI36
NG_008880.1:g.107610C>T , LRG_627:g.107610C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378444.9:c.626C>T MANE Select	ENSP00000367705.4:p.Ser209Leu
ENST00000406200.4:c.626C>T	ENSP00000384485.3:p.Ser209Leu
ENST00000413905.6:c.626C>T	ENSP00000408006.2:p.Ser209Leu
ENST00000427012.3:c.626C>T	ENSP00000403823.3:p.Ser209Leu
ENST00000442018.6:c.626C>T	ENSP00000387552.2:p.Ser209Leu
ENST00000615339.2:c.626C>T	ENSP00000483217.2:p.Ser209Leu
ENST00000672922.2:c.626C>T	ENSP00000499892.2:p.Ser209Leu
ENST00000673391.1:c.626C>T	ENSP00000500446.1:p.Ser209Leu
ENST00000679513.1:c.626C>T	ENSP00000505761.1:p.Ser209Leu
ENST00000680831.1:c.626C>T	ENSP00000505507.1:p.Ser209Leu
ENST00000342274.8:c.626C>T	ENSP00000345923.4:p.Ser209Leu
ENST00000378444.8:c.626C>T	ENSP00000367705.4:p.Ser209Leu
ENST00000378455.8:c.626C>T	ENSP00000367716.4:p.Ser209Leu
ENST00000397354.7:c.626C>T	ENSP00000380512.3:p.Ser209Leu
ENST00000406200.2:c.626C>T	ENSP00000384485.2:p.Ser209Leu
ENST00000490976.5:n.666C>T
ENST00000615339.1:c.22-1175C>T	ENSP00000483217.1:n.22-1175C>T
NM_001123383.1:c.626C>T , LRG_627t1:c.626C>T	NP_001116855.1:p.Ser209Leu
NM_001123384.1:c.626C>T	NP_001116856.1:p.Ser209Leu
NM_001123385.1:c.626C>T , LRG_627t2:c.626C>T	NP_001116857.1:p.Ser209Leu
NM_017745.5:c.626C>T	NP_060215.4:p.Ser209Leu
XM_005272616.1:c.626C>T	XP_005272673.1:p.Ser209Leu
XM_005272618.2:c.626C>T	XP_005272675.1:p.Ser209Leu
XM_005272619.3:c.626C>T	XP_005272676.1:p.Ser209Leu
XM_005272620.3:c.626C>T	XP_005272677.1:p.Ser209Leu
XM_006724536.2:c.626C>T	XP_006724599.1:p.Ser209Leu
XM_011543929.1:c.626C>T	XP_011542231.1:p.Ser209Leu
XM_011543930.1:c.626C>T	XP_011542232.1:p.Ser209Leu
XM_011543931.1:c.626C>T	XP_011542233.1:p.Ser209Leu
XM_005272618.3:c.626C>T	XP_005272675.1:p.Ser209Leu
XM_005272619.4:c.626C>T	XP_005272676.1:p.Ser209Leu
XM_005272620.4:c.626C>T	XP_005272677.1:p.Ser209Leu
XM_006724536.3:c.626C>T	XP_006724599.1:p.Ser209Leu
XM_011543929.2:c.626C>T	XP_011542231.1:p.Ser209Leu
XM_011543931.2:c.626C>T	XP_011542233.1:p.Ser209Leu
XM_017029615.1:c.626C>T	XP_016885104.1:p.Ser209Leu
XM_017029616.2:c.626C>T	XP_016885105.1:p.Ser209Leu
NM_001123384.2:c.626C>T	NP_001116856.1:p.Ser209Leu
NM_001123385.2:c.626C>T MANE Select	NP_001116857.1:p.Ser209Leu
NM_017745.6:c.626C>T	NP_060215.4:p.Ser209Leu