Canonical Allele Identifier: CA2666006832

Gene: BAP1

Linked Data

• gnomAD v4: 3-52402526-GAGGCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402530_52402534del , CM000665.2:g.52402530_52402534del	GRCh38
NC_000003.11:g.52436546_52436550del , CM000665.1:g.52436546_52436550del	GRCh37
NC_000003.10:g.52411586_52411590del	NCBI36
NG_031859.1:g.12463_12467del , LRG_529:g.12463_12467del

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.2056+71_2056+75del MANE Select	ENSP00000417132.1:n.2056+71_2056+75del
ENST00000296288.9:c.2002+71_2002+75del	ENSP00000296288.5:n.2002+71_2002+75del
ENST00000460680.5:c.2056+71_2056+75del	ENSP00000417132.1:n.2056+71_2056+75del
ENST00000466093.1:n.729+71_729+75del
ENST00000469613.5:c.255+71_255+75del
ENST00000478368.1:c.628+71_628+75del	ENSP00000420647.1:n.628+71_628+75del
NM_004656.3:c.2056+71_2056+75del	NP_004647.1:n.2056+71_2056+75del
XM_011534149.1:c.2125+71_2125+75del	XP_011532451.1:n.2125+71_2125+75del
XM_011534150.1:c.2080+71_2080+75del	XP_011532452.1:n.2080+71_2080+75del
XM_011534151.1:c.2071+71_2071+75del	XP_011532453.1:n.2071+71_2071+75del
XM_011534152.1:c.2011+71_2011+75del	XP_011532454.1:n.2011+71_2011+75del
XM_011534149.3:c.2125+71_2125+75del	XP_011532451.1:n.2125+71_2125+75del
XM_011534150.3:c.2080+71_2080+75del	XP_011532452.1:n.2080+71_2080+75del
XM_011534151.3:c.2071+71_2071+75del	XP_011532453.1:n.2071+71_2071+75del
XM_011534152.2:c.2011+71_2011+75del	XP_011532454.1:n.2011+71_2011+75del
XM_017007303.2:c.2002+71_2002+75del	XP_016862792.1:n.2002+71_2002+75del
NM_004656.4:c.2056+71_2056+75del MANE Select	NP_004647.1:n.2056+71_2056+75del