Canonical Allele Identifier: CA645529902

Gene: BAP1

Linked Data

• ClinVar Variation Id: 1422258
• ClinVar RCV Id: RCV001919446
• dbSNP Id: rs2153226608
• COSMIC: COSM5325085

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403486del , CM000665.2:g.52403486del	GRCh38
NC_000003.11:g.52437502del , CM000665.1:g.52437502del	GRCh37
NC_000003.10:g.52412542del	NCBI36
NG_031859.1:g.11510del , LRG_529:g.11510del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1661del MANE Select	ENSP00000417132.1:p.Gly554ValfsTer17
ENST00000296288.9:c.1607del	ENSP00000296288.5:p.Gly536ValfsTer17
ENST00000460680.5:c.1661del	ENSP00000417132.1:p.Gly554ValfsTer17
ENST00000466093.1:n.68del
ENST00000469613.5:c.119+317del
ENST00000478368.1:c.164del	ENSP00000420647.1:p.Gly55ValfsTer17
NM_004656.3:c.1661del	NP_004647.1:p.Gly554ValfsTer17
XM_011534149.1:c.1661del	XP_011532451.1:p.Gly554ValfsTer17
XM_011534150.1:c.1661del	XP_011532452.1:p.Gly554ValfsTer17
XM_011534151.1:c.1607del	XP_011532453.1:p.Gly536ValfsTer17
XM_011534152.1:c.1661del	XP_011532454.1:p.Gly554ValfsTer17
XM_011534149.3:c.1661del	XP_011532451.1:p.Gly554ValfsTer17
XM_011534150.3:c.1661del	XP_011532452.1:p.Gly554ValfsTer17
XM_011534151.3:c.1607del	XP_011532453.1:p.Gly536ValfsTer17
XM_011534152.2:c.1661del	XP_011532454.1:p.Gly554ValfsTer17
XM_017007303.2:c.1607del	XP_016862792.1:p.Gly536ValfsTer17
NM_004656.4:c.1661del MANE Select	NP_004647.1:p.Gly554ValfsTer17