Canonical Allele Identifier: CA645529914

Gene: BAP1

Linked Data

• COSMIC: COSM4411165

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403733dup , CM000665.2:g.52403733dup	GRCh38
NC_000003.11:g.52437749dup , CM000665.1:g.52437749dup	GRCh37
NC_000003.10:g.52412789dup	NCBI36
NG_031859.1:g.11261dup , LRG_529:g.11261dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.1412dup MANE Select	ENSP00000417132.1:p.Gly472TrpfsTer20
ENST00000296288.9:c.1358dup	ENSP00000296288.5:p.Gly454TrpfsTer20
ENST00000460680.5:c.1412dup	ENSP00000417132.1:p.Gly472TrpfsTer20
ENST00000469613.5:c.119+68dup
ENST00000490804.1:n.840dup
NM_004656.3:c.1412dup	NP_004647.1:p.Gly472TrpfsTer20
XM_011534149.1:c.1412dup	XP_011532451.1:p.Gly472TrpfsTer20
XM_011534150.1:c.1412dup	XP_011532452.1:p.Gly472TrpfsTer20
XM_011534151.1:c.1358dup	XP_011532453.1:p.Gly454TrpfsTer20
XM_011534152.1:c.1412dup	XP_011532454.1:p.Gly472TrpfsTer20
XM_011534149.3:c.1412dup	XP_011532451.1:p.Gly472TrpfsTer20
XM_011534150.3:c.1412dup	XP_011532452.1:p.Gly472TrpfsTer20
XM_011534151.3:c.1358dup	XP_011532453.1:p.Gly454TrpfsTer20
XM_011534152.2:c.1412dup	XP_011532454.1:p.Gly472TrpfsTer20
XM_017007303.2:c.1358dup	XP_016862792.1:p.Gly454TrpfsTer20
NM_004656.4:c.1412dup MANE Select	NP_004647.1:p.Gly472TrpfsTer20