Canonical Allele Identifier: CA1364834902

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402665G= , CM000665.2:g.52402665G=	GRCh38
NC_000003.11:g.52436681G= , CM000665.1:g.52436681G=	GRCh37
NC_000003.10:g.52411721G=	NCBI36
NG_031859.1:g.12329C= , LRG_529:g.12329C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1993C= MANE Select	ENSP00000417132.1:p.Gln665=
ENST00000296288.9:c.1939C=	ENSP00000296288.5:p.Gln647=
ENST00000460680.5:c.1993C=	ENSP00000417132.1:p.Gln665=
ENST00000466093.1:n.666C=
ENST00000469613.5:c.192C=
ENST00000478368.1:c.565C=	ENSP00000420647.1:p.Gln189=
NM_004656.3:c.1993C=	NP_004647.1:p.Gln665=
XM_011534149.1:c.2062C=	XP_011532451.1:p.Gln688=
XM_011534150.1:c.2017C=	XP_011532452.1:p.Gln673=
XM_011534151.1:c.2008C=	XP_011532453.1:p.Gln670=
XM_011534152.1:c.1948C=	XP_011532454.1:p.Gln650=
XM_011534149.3:c.2062C=	XP_011532451.1:p.Gln688=
XM_011534150.3:c.2017C=	XP_011532452.1:p.Gln673=
XM_011534151.3:c.2008C=	XP_011532453.1:p.Gln670=
XM_011534152.2:c.1948C=	XP_011532454.1:p.Gln650=
XM_017007303.2:c.1939C=	XP_016862792.1:p.Gln647=
NM_004656.4:c.1993C= MANE Select	NP_004647.1:p.Gln665=