Canonical Allele Identifier: CA1364834530

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402362T= , CM000665.2:g.52402362T=	GRCh38
NC_000003.11:g.52436378T= , CM000665.1:g.52436378T=	GRCh37
NC_000003.10:g.52411418T=	NCBI36
NG_031859.1:g.12632A= , LRG_529:g.12632A=
NG_052911.1:g.91044T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2116A= MANE Select	ENSP00000417132.1:p.Ile706=
ENST00000296288.9:c.2062A=	ENSP00000296288.5:p.Ile688=
ENST00000460680.5:c.2116A=	ENSP00000417132.1:p.Ile706=
ENST00000466093.1:n.789A=
ENST00000469613.5:c.315A=
ENST00000478368.1:c.688A=	ENSP00000420647.1:p.Ile230=
NM_004656.3:c.2116A=	NP_004647.1:p.Ile706=
XM_011534149.1:c.2185A=	XP_011532451.1:p.Ile729=
XM_011534150.1:c.2140A=	XP_011532452.1:p.Ile714=
XM_011534151.1:c.2131A=	XP_011532453.1:p.Ile711=
XM_011534152.1:c.2071A=	XP_011532454.1:p.Ile691=
XM_011534149.3:c.2185A=	XP_011532451.1:p.Ile729=
XM_011534150.3:c.2140A=	XP_011532452.1:p.Ile714=
XM_011534151.3:c.2131A=	XP_011532453.1:p.Ile711=
XM_011534152.2:c.2071A=	XP_011532454.1:p.Ile691=
XM_017007303.2:c.2062A=	XP_016862792.1:p.Ile688=
NM_004656.4:c.2116A= MANE Select	NP_004647.1:p.Ile706=