Canonical Allele Identifier: CA3065057059

Gene: BCOR

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.40064370A= , CM000685.2:g.40064370A=	GRCh38
NC_000023.10:g.39923623A= , CM000685.1:g.39923623A=	GRCh37
NC_000023.9:g.39808567A=	NCBI36
NG_008880.1:g.117960T= , LRG_627:g.117960T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378444.9:c.3468T= MANE Select	ENSP00000367705.4:p.Pro1156=
ENST00000406200.4:c.3468T=	ENSP00000384485.3:p.Pro1156=
ENST00000413905.6:c.3468T=	ENSP00000408006.2:p.Pro1156=
ENST00000427012.3:c.3414T=	ENSP00000403823.3:p.Pro1138=
ENST00000442018.6:c.3468T=	ENSP00000387552.2:p.Pro1156=
ENST00000615339.2:c.3468T=	ENSP00000483217.2:p.Pro1156=
ENST00000672922.2:c.3468T=	ENSP00000499892.2:p.Pro1156=
ENST00000673391.1:c.3468T=	ENSP00000500446.1:p.Pro1156=
ENST00000679513.1:c.3468T=	ENSP00000505761.1:p.Pro1156=
ENST00000680831.1:c.3468T=	ENSP00000505507.1:p.Pro1156=
ENST00000342274.8:c.3468T=	ENSP00000345923.4:p.Pro1156=
ENST00000378444.8:c.3468T=	ENSP00000367705.4:p.Pro1156=
ENST00000378455.8:c.3414T=	ENSP00000367716.4:p.Pro1138=
ENST00000378463.5:c.99T=	ENSP00000367724.1:p.Pro33=
ENST00000397354.7:c.3468T=	ENSP00000380512.3:p.Pro1156=
ENST00000406200.2:c.3468T=	ENSP00000384485.2:p.Pro1156=
ENST00000413905.5:c.180T=	ENSP00000408006.1:p.Pro60=
NM_001123383.1:c.3468T= , LRG_627t1:c.3468T=	NP_001116855.1:p.Pro1156=
NM_001123384.1:c.3414T=	NP_001116856.1:p.Pro1138=
NM_001123385.1:c.3468T= , LRG_627t2:c.3468T=	NP_001116857.1:p.Pro1156=
NM_017745.5:c.3468T=	NP_060215.4:p.Pro1156=
XM_005272616.1:c.3468T=	XP_005272673.1:p.Pro1156=
XM_005272618.2:c.3468T=	XP_005272675.1:p.Pro1156=
XM_005272619.3:c.3414T=	XP_005272676.1:p.Pro1138=
XM_005272620.3:c.3414T=	XP_005272677.1:p.Pro1138=
XM_006724536.2:c.3468T=	XP_006724599.1:p.Pro1156=
XM_011543929.1:c.3468T=	XP_011542231.1:p.Pro1156=
XM_011543930.1:c.3468T=	XP_011542232.1:p.Pro1156=
XM_011543931.1:c.3468T=	XP_011542233.1:p.Pro1156=
XM_005272618.3:c.3468T=	XP_005272675.1:p.Pro1156=
XM_005272619.4:c.3414T=	XP_005272676.1:p.Pro1138=
XM_005272620.4:c.3414T=	XP_005272677.1:p.Pro1138=
XM_006724536.3:c.3468T=	XP_006724599.1:p.Pro1156=
XM_011543929.2:c.3468T=	XP_011542231.1:p.Pro1156=
XM_011543931.2:c.3468T=	XP_011542233.1:p.Pro1156=
XM_017029615.1:c.3468T=	XP_016885104.1:p.Pro1156=
XM_017029616.2:c.3468T=	XP_016885105.1:p.Pro1156=
NM_001123384.2:c.3414T=	NP_001116856.1:p.Pro1138=
NM_001123385.2:c.3468T= MANE Select	NP_001116857.1:p.Pro1156=
NM_017745.6:c.3468T=	NP_060215.4:p.Pro1156=