Canonical Allele Identifier: CA1364834549

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402375G= , CM000665.2:g.52402375G=	GRCh38
NC_000003.11:g.52436391G= , CM000665.1:g.52436391G=	GRCh37
NC_000003.10:g.52411431G=	NCBI36
NG_031859.1:g.12619C= , LRG_529:g.12619C=
NG_052911.1:g.91057G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2103C= MANE Select	ENSP00000417132.1:p.Arg701=
ENST00000296288.9:c.2049C=	ENSP00000296288.5:p.Arg683=
ENST00000460680.5:c.2103C=	ENSP00000417132.1:p.Arg701=
ENST00000466093.1:n.776C=
ENST00000469613.5:c.302C=
ENST00000478368.1:c.675C=	ENSP00000420647.1:p.Arg225=
NM_004656.3:c.2103C=	NP_004647.1:p.Arg701=
XM_011534149.1:c.2172C=	XP_011532451.1:p.Arg724=
XM_011534150.1:c.2127C=	XP_011532452.1:p.Arg709=
XM_011534151.1:c.2118C=	XP_011532453.1:p.Arg706=
XM_011534152.1:c.2058C=	XP_011532454.1:p.Arg686=
XM_011534149.3:c.2172C=	XP_011532451.1:p.Arg724=
XM_011534150.3:c.2127C=	XP_011532452.1:p.Arg709=
XM_011534151.3:c.2118C=	XP_011532453.1:p.Arg706=
XM_011534152.2:c.2058C=	XP_011532454.1:p.Arg686=
XM_017007303.2:c.2049C=	XP_016862792.1:p.Arg683=
NM_004656.4:c.2103C= MANE Select	NP_004647.1:p.Arg701=