Canonical Allele Identifier: CA2702828499

Gene: BAP1

Linked Data

• dbSNP Id: rs2153226259

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402735del , CM000665.2:g.52402735del	GRCh38
NC_000003.11:g.52436751del , CM000665.1:g.52436751del	GRCh37
NC_000003.10:g.52411791del	NCBI36
NG_031859.1:g.12260del , LRG_529:g.12260del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1983+45del MANE Select	ENSP00000417132.1:n.1983+45del
ENST00000296288.9:c.1929+45del	ENSP00000296288.5:n.1929+45del
ENST00000460680.5:c.1983+45del	ENSP00000417132.1:n.1983+45del
ENST00000466093.1:n.656+45del
ENST00000469613.5:c.182+45del
ENST00000478368.1:c.555+45del	ENSP00000420647.1:n.555+45del
NM_004656.3:c.1983+45del	NP_004647.1:n.1983+45del
XM_011534149.1:c.2052+45del	XP_011532451.1:n.2052+45del
XM_011534150.1:c.2007+45del	XP_011532452.1:n.2007+45del
XM_011534151.1:c.1998+45del	XP_011532453.1:n.1998+45del
XM_011534152.1:c.1938+45del	XP_011532454.1:n.1938+45del
XM_011534149.3:c.2052+45del	XP_011532451.1:n.2052+45del
XM_011534150.3:c.2007+45del	XP_011532452.1:n.2007+45del
XM_011534151.3:c.1998+45del	XP_011532453.1:n.1998+45del
XM_011534152.2:c.1938+45del	XP_011532454.1:n.1938+45del
XM_017007303.2:c.1929+45del	XP_016862792.1:n.1929+45del
NM_004656.4:c.1983+45del MANE Select	NP_004647.1:n.1983+45del