Canonical Allele Identifier: CA645529853

Gene: BAP1

Linked Data

• COSMIC: COSM1169642

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402371dup , CM000665.2:g.52402371dup	GRCh38
NC_000003.11:g.52436387dup , CM000665.1:g.52436387dup	GRCh37
NC_000003.10:g.52411427dup	NCBI36
NG_031859.1:g.12626dup , LRG_529:g.12626dup
NG_052911.1:g.91053dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2110dup MANE Select	ENSP00000417132.1:p.Val704GlyfsTer13
ENST00000296288.9:c.2056dup	ENSP00000296288.5:p.Val686GlyfsTer13
ENST00000460680.5:c.2110dup	ENSP00000417132.1:p.Val704GlyfsTer13
ENST00000466093.1:n.783dup
ENST00000469613.5:c.309dup
ENST00000478368.1:c.682dup	ENSP00000420647.1:p.Val228GlyfsTer13
NM_004656.3:c.2110dup	NP_004647.1:p.Val704GlyfsTer13
XM_011534149.1:c.2179dup	XP_011532451.1:p.Val727GlyfsTer13
XM_011534150.1:c.2134dup	XP_011532452.1:p.Val712GlyfsTer13
XM_011534151.1:c.2125dup	XP_011532453.1:p.Val709GlyfsTer13
XM_011534152.1:c.2065dup	XP_011532454.1:p.Val689GlyfsTer13
XM_011534149.3:c.2179dup	XP_011532451.1:p.Val727GlyfsTer13
XM_011534150.3:c.2134dup	XP_011532452.1:p.Val712GlyfsTer13
XM_011534151.3:c.2125dup	XP_011532453.1:p.Val709GlyfsTer13
XM_011534152.2:c.2065dup	XP_011532454.1:p.Val689GlyfsTer13
XM_017007303.2:c.2056dup	XP_016862792.1:p.Val686GlyfsTer13
NM_004656.4:c.2110dup MANE Select	NP_004647.1:p.Val704GlyfsTer13