Canonical Allele Identifier: CA1364834742

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402522A= , CM000665.2:g.52402522A=	GRCh38
NC_000003.11:g.52436538A= , CM000665.1:g.52436538A=	GRCh37
NC_000003.10:g.52411578A=	NCBI36
NG_031859.1:g.12472T= , LRG_529:g.12472T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.2056+80T= MANE Select	ENSP00000417132.1:n.2056+80T=
ENST00000296288.9:c.2002+80T=	ENSP00000296288.5:n.2002+80T=
ENST00000460680.5:c.2056+80T=	ENSP00000417132.1:n.2056+80T=
ENST00000466093.1:n.729+80T=
ENST00000469613.5:c.255+80T=
ENST00000478368.1:c.628+80T=	ENSP00000420647.1:n.628+80T=
NM_004656.3:c.2056+80T=	NP_004647.1:n.2056+80T=
XM_011534149.1:c.2125+80T=	XP_011532451.1:n.2125+80T=
XM_011534150.1:c.2080+80T=	XP_011532452.1:n.2080+80T=
XM_011534151.1:c.2071+80T=	XP_011532453.1:n.2071+80T=
XM_011534152.1:c.2011+80T=	XP_011532454.1:n.2011+80T=
XM_011534149.3:c.2125+80T=	XP_011532451.1:n.2125+80T=
XM_011534150.3:c.2080+80T=	XP_011532452.1:n.2080+80T=
XM_011534151.3:c.2071+80T=	XP_011532453.1:n.2071+80T=
XM_011534152.2:c.2011+80T=	XP_011532454.1:n.2011+80T=
XM_017007303.2:c.2002+80T=	XP_016862792.1:n.2002+80T=
NM_004656.4:c.2056+80T= MANE Select	NP_004647.1:n.2056+80T=