Canonical Allele Identifier: CA1364834827

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402608G= , CM000665.2:g.52402608G=	GRCh38
NC_000003.11:g.52436624G= , CM000665.1:g.52436624G=	GRCh37
NC_000003.10:g.52411664G=	NCBI36
NG_031859.1:g.12386C= , LRG_529:g.12386C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2050C= MANE Select	ENSP00000417132.1:p.Gln684=
ENST00000296288.9:c.1996C=	ENSP00000296288.5:p.Gln666=
ENST00000460680.5:c.2050C=	ENSP00000417132.1:p.Gln684=
ENST00000466093.1:n.723C=
ENST00000469613.5:c.249C=
ENST00000478368.1:c.622C=	ENSP00000420647.1:p.Gln208=
NM_004656.3:c.2050C=	NP_004647.1:p.Gln684=
XM_011534149.1:c.2119C=	XP_011532451.1:p.Gln707=
XM_011534150.1:c.2074C=	XP_011532452.1:p.Gln692=
XM_011534151.1:c.2065C=	XP_011532453.1:p.Gln689=
XM_011534152.1:c.2005C=	XP_011532454.1:p.Gln669=
XM_011534149.3:c.2119C=	XP_011532451.1:p.Gln707=
XM_011534150.3:c.2074C=	XP_011532452.1:p.Gln692=
XM_011534151.3:c.2065C=	XP_011532453.1:p.Gln689=
XM_011534152.2:c.2005C=	XP_011532454.1:p.Gln669=
XM_017007303.2:c.1996C=	XP_016862792.1:p.Gln666=
NM_004656.4:c.2050C= MANE Select	NP_004647.1:p.Gln684=