Canonical Allele Identifier: CA1364834925

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402668C= , CM000665.2:g.52402668C=	GRCh38
NC_000003.11:g.52436684C= , CM000665.1:g.52436684C=	GRCh37
NC_000003.10:g.52411724C=	NCBI36
NG_031859.1:g.12326G= , LRG_529:g.12326G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1990G= MANE Select	ENSP00000417132.1:p.Asp664=
ENST00000296288.9:c.1936G=	ENSP00000296288.5:p.Asp646=
ENST00000460680.5:c.1990G=	ENSP00000417132.1:p.Asp664=
ENST00000466093.1:n.663G=
ENST00000469613.5:c.189G=
ENST00000478368.1:c.562G=	ENSP00000420647.1:p.Asp188=
NM_004656.3:c.1990G=	NP_004647.1:p.Asp664=
XM_011534149.1:c.2059G=	XP_011532451.1:p.Asp687=
XM_011534150.1:c.2014G=	XP_011532452.1:p.Asp672=
XM_011534151.1:c.2005G=	XP_011532453.1:p.Asp669=
XM_011534152.1:c.1945G=	XP_011532454.1:p.Asp649=
XM_011534149.3:c.2059G=	XP_011532451.1:p.Asp687=
XM_011534150.3:c.2014G=	XP_011532452.1:p.Asp672=
XM_011534151.3:c.2005G=	XP_011532453.1:p.Asp669=
XM_011534152.2:c.1945G=	XP_011532454.1:p.Asp649=
XM_017007303.2:c.1936G=	XP_016862792.1:p.Asp646=
NM_004656.4:c.1990G= MANE Select	NP_004647.1:p.Asp664=