Canonical Allele Identifier: CA1364834639

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402419T= , CM000665.2:g.52402419T=	GRCh38
NC_000003.11:g.52436435T= , CM000665.1:g.52436435T=	GRCh37
NC_000003.10:g.52411475T=	NCBI36
NG_031859.1:g.12575A= , LRG_529:g.12575A=
NG_052911.1:g.91101T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2059A= MANE Select	ENSP00000417132.1:p.Met687=
ENST00000296288.9:c.2005A=	ENSP00000296288.5:p.Met669=
ENST00000460680.5:c.2059A=	ENSP00000417132.1:p.Met687=
ENST00000466093.1:n.732A=
ENST00000469613.5:c.258A=
ENST00000478368.1:c.631A=	ENSP00000420647.1:p.Met211=
NM_004656.3:c.2059A=	NP_004647.1:p.Met687=
XM_011534149.1:c.2128A=	XP_011532451.1:p.Met710=
XM_011534150.1:c.2083A=	XP_011532452.1:p.Met695=
XM_011534151.1:c.2074A=	XP_011532453.1:p.Met692=
XM_011534152.1:c.2014A=	XP_011532454.1:p.Met672=
XM_011534149.3:c.2128A=	XP_011532451.1:p.Met710=
XM_011534150.3:c.2083A=	XP_011532452.1:p.Met695=
XM_011534151.3:c.2074A=	XP_011532453.1:p.Met692=
XM_011534152.2:c.2014A=	XP_011532454.1:p.Met672=
XM_017007303.2:c.2005A=	XP_016862792.1:p.Met669=
NM_004656.4:c.2059A= MANE Select	NP_004647.1:p.Met687=