Canonical Allele Identifier: CA516346287
Gene: BCOR HGNC NCBI

Linked Data

dbSNP Id: rs1392691539
MyVariant Identifiers: chrX:g.39933363C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.40074110C>T , CM000685.2:g.40074110C>T GRCh38
NC_000023.10:g.39933363C>T , CM000685.1:g.39933363C>T GRCh37
NC_000023.9:g.39818307C>T NCBI36
NG_008880.1:g.108220G>A , LRG_627:g.108220G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378444.9:c.1236G>A MANE Select ENSP00000367705.4:p.Lys412=
ENST00000406200.4:c.1236G>A ENSP00000384485.3:p.Lys412=
ENST00000413905.6:c.1236G>A ENSP00000408006.2:p.Lys412=
ENST00000427012.3:c.1236G>A ENSP00000403823.3:p.Lys412=
ENST00000442018.6:c.1236G>A ENSP00000387552.2:p.Lys412=
ENST00000615339.2:c.1236G>A ENSP00000483217.2:p.Lys412=
ENST00000672922.2:c.1236G>A ENSP00000499892.2:p.Lys412=
ENST00000673391.1:c.1236G>A ENSP00000500446.1:p.Lys412=
ENST00000679513.1:c.1236G>A ENSP00000505761.1:p.Lys412=
ENST00000680831.1:c.1236G>A ENSP00000505507.1:p.Lys412=
ENST00000342274.8:c.1236G>A ENSP00000345923.4:p.Lys412=
ENST00000378444.8:c.1236G>A ENSP00000367705.4:p.Lys412=
ENST00000378455.8:c.1236G>A ENSP00000367716.4:p.Lys412=
ENST00000397354.7:c.1236G>A ENSP00000380512.3:p.Lys412=
ENST00000406200.2:c.1236G>A ENSP00000384485.2:p.Lys412=
ENST00000490976.5:n.1276G>A
ENST00000615339.1:c.22-565G>A ENSP00000483217.1:n.22-565G>A
NM_001123383.1:c.1236G>A , LRG_627t1:c.1236G>A NP_001116855.1:p.Lys412=
NM_001123384.1:c.1236G>A NP_001116856.1:p.Lys412=
NM_001123385.1:c.1236G>A , LRG_627t2:c.1236G>A NP_001116857.1:p.Lys412=
NM_017745.5:c.1236G>A NP_060215.4:p.Lys412=
XM_005272616.1:c.1236G>A XP_005272673.1:p.Lys412=
XM_005272618.2:c.1236G>A XP_005272675.1:p.Lys412=
XM_005272619.3:c.1236G>A XP_005272676.1:p.Lys412=
XM_005272620.3:c.1236G>A XP_005272677.1:p.Lys412=
XM_006724536.2:c.1236G>A XP_006724599.1:p.Lys412=
XM_011543929.1:c.1236G>A XP_011542231.1:p.Lys412=
XM_011543930.1:c.1236G>A XP_011542232.1:p.Lys412=
XM_011543931.1:c.1236G>A XP_011542233.1:p.Lys412=
XM_005272618.3:c.1236G>A XP_005272675.1:p.Lys412=
XM_005272619.4:c.1236G>A XP_005272676.1:p.Lys412=
XM_005272620.4:c.1236G>A XP_005272677.1:p.Lys412=
XM_006724536.3:c.1236G>A XP_006724599.1:p.Lys412=
XM_011543929.2:c.1236G>A XP_011542231.1:p.Lys412=
XM_011543931.2:c.1236G>A XP_011542233.1:p.Lys412=
XM_017029615.1:c.1236G>A XP_016885104.1:p.Lys412=
XM_017029616.2:c.1236G>A XP_016885105.1:p.Lys412=
NM_001123384.2:c.1236G>A NP_001116856.1:p.Lys412=
NM_001123385.2:c.1236G>A MANE Select NP_001116857.1:p.Lys412=
NM_017745.6:c.1236G>A NP_060215.4:p.Lys412=