Canonical Allele Identifier: CA1364834866

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402652T= , CM000665.2:g.52402652T=	GRCh38
NC_000003.11:g.52436668T= , CM000665.1:g.52436668T=	GRCh37
NC_000003.10:g.52411708T=	NCBI36
NG_031859.1:g.12342A= , LRG_529:g.12342A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2006A= MANE Select	ENSP00000417132.1:p.His669=
ENST00000296288.9:c.1952A=	ENSP00000296288.5:p.His651=
ENST00000460680.5:c.2006A=	ENSP00000417132.1:p.His669=
ENST00000466093.1:n.679A=
ENST00000469613.5:c.205A=
ENST00000478368.1:c.578A=	ENSP00000420647.1:p.His193=
NM_004656.3:c.2006A=	NP_004647.1:p.His669=
XM_011534149.1:c.2075A=	XP_011532451.1:p.His692=
XM_011534150.1:c.2030A=	XP_011532452.1:p.His677=
XM_011534151.1:c.2021A=	XP_011532453.1:p.His674=
XM_011534152.1:c.1961A=	XP_011532454.1:p.His654=
XM_011534149.3:c.2075A=	XP_011532451.1:p.His692=
XM_011534150.3:c.2030A=	XP_011532452.1:p.His677=
XM_011534151.3:c.2021A=	XP_011532453.1:p.His674=
XM_011534152.2:c.1961A=	XP_011532454.1:p.His654=
XM_017007303.2:c.1952A=	XP_016862792.1:p.His651=
NM_004656.4:c.2006A= MANE Select	NP_004647.1:p.His669=