Canonical Allele Identifier: CA2560251986

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403723_52403731del , CM000665.2:g.52403723_52403731del	GRCh38
NC_000003.11:g.52437739_52437747del , CM000665.1:g.52437739_52437747del	GRCh37
NC_000003.10:g.52412779_52412787del	NCBI36
NG_031859.1:g.11264_11272del , LRG_529:g.11264_11272del

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.1415_1423del MANE Select	ENSP00000417132.1:p.Gly472_Pro474del
ENST00000296288.9:c.1361_1369del	ENSP00000296288.5:p.Gly454_Pro456del
ENST00000460680.5:c.1415_1423del	ENSP00000417132.1:p.Gly472_Pro474del
ENST00000469613.5:c.119+71_119+79del
ENST00000490804.1:n.843_851del
NM_004656.3:c.1415_1423del	NP_004647.1:p.Gly472_Pro474del
XM_011534149.1:c.1415_1423del	XP_011532451.1:p.Gly472_Pro474del
XM_011534150.1:c.1415_1423del	XP_011532452.1:p.Gly472_Pro474del
XM_011534151.1:c.1361_1369del	XP_011532453.1:p.Gly454_Pro456del
XM_011534152.1:c.1415_1423del	XP_011532454.1:p.Gly472_Pro474del
XM_011534149.3:c.1415_1423del	XP_011532451.1:p.Gly472_Pro474del
XM_011534150.3:c.1415_1423del	XP_011532452.1:p.Gly472_Pro474del
XM_011534151.3:c.1361_1369del	XP_011532453.1:p.Gly454_Pro456del
XM_011534152.2:c.1415_1423del	XP_011532454.1:p.Gly472_Pro474del
XM_017007303.2:c.1361_1369del	XP_016862792.1:p.Gly454_Pro456del
NM_004656.4:c.1415_1423del MANE Select	NP_004647.1:p.Gly472_Pro474del