Canonical Allele Identifier: CA1364834892

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402659T= , CM000665.2:g.52402659T=	GRCh38
NC_000003.11:g.52436675T= , CM000665.1:g.52436675T=	GRCh37
NC_000003.10:g.52411715T=	NCBI36
NG_031859.1:g.12335A= , LRG_529:g.12335A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1999A= MANE Select	ENSP00000417132.1:p.Arg667=
ENST00000296288.9:c.1945A=	ENSP00000296288.5:p.Arg649=
ENST00000460680.5:c.1999A=	ENSP00000417132.1:p.Arg667=
ENST00000466093.1:n.672A=
ENST00000469613.5:c.198A=
ENST00000478368.1:c.571A=	ENSP00000420647.1:p.Arg191=
NM_004656.3:c.1999A=	NP_004647.1:p.Arg667=
XM_011534149.1:c.2068A=	XP_011532451.1:p.Arg690=
XM_011534150.1:c.2023A=	XP_011532452.1:p.Arg675=
XM_011534151.1:c.2014A=	XP_011532453.1:p.Arg672=
XM_011534152.1:c.1954A=	XP_011532454.1:p.Arg652=
XM_011534149.3:c.2068A=	XP_011532451.1:p.Arg690=
XM_011534150.3:c.2023A=	XP_011532452.1:p.Arg675=
XM_011534151.3:c.2014A=	XP_011532453.1:p.Arg672=
XM_011534152.2:c.1954A=	XP_011532454.1:p.Arg652=
XM_017007303.2:c.1945A=	XP_016862792.1:p.Arg649=
NM_004656.4:c.1999A= MANE Select	NP_004647.1:p.Arg667=