Canonical Allele Identifier: CA1364834656

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402432G= , CM000665.2:g.52402432G=	GRCh38
NC_000003.11:g.52436448G= , CM000665.1:g.52436448G=	GRCh37
NC_000003.10:g.52411488G=	NCBI36
NG_031859.1:g.12562C= , LRG_529:g.12562C=
NG_052911.1:g.91114G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.2057-11C= MANE Select	ENSP00000417132.1:n.2057-11C=
ENST00000296288.9:c.2003-11C=	ENSP00000296288.5:n.2003-11C=
ENST00000460680.5:c.2057-11C=	ENSP00000417132.1:n.2057-11C=
ENST00000466093.1:n.730-11C=
ENST00000469613.5:c.256-11C=
ENST00000478368.1:c.629-11C=	ENSP00000420647.1:n.629-11C=
NM_004656.3:c.2057-11C=	NP_004647.1:n.2057-11C=
XM_011534149.1:c.2126-11C=	XP_011532451.1:n.2126-11C=
XM_011534150.1:c.2081-11C=	XP_011532452.1:n.2081-11C=
XM_011534151.1:c.2072-11C=	XP_011532453.1:n.2072-11C=
XM_011534152.1:c.2012-11C=	XP_011532454.1:n.2012-11C=
XM_011534149.3:c.2126-11C=	XP_011532451.1:n.2126-11C=
XM_011534150.3:c.2081-11C=	XP_011532452.1:n.2081-11C=
XM_011534151.3:c.2072-11C=	XP_011532453.1:n.2072-11C=
XM_011534152.2:c.2012-11C=	XP_011532454.1:n.2012-11C=
XM_017007303.2:c.2003-11C=	XP_016862792.1:n.2003-11C=
NM_004656.4:c.2057-11C= MANE Select	NP_004647.1:n.2057-11C=