Canonical Allele Identifier: CA1364834508

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402351G= , CM000665.2:g.52402351G=	GRCh38
NC_000003.11:g.52436367G= , CM000665.1:g.52436367G=	GRCh37
NC_000003.10:g.52411407G=	NCBI36
NG_031859.1:g.12643C= , LRG_529:g.12643C=
NG_052911.1:g.91033G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2127C= MANE Select	ENSP00000417132.1:p.Leu709=
ENST00000296288.9:c.2073C=	ENSP00000296288.5:p.Leu691=
ENST00000460680.5:c.2127C=	ENSP00000417132.1:p.Leu709=
ENST00000466093.1:n.800C=
ENST00000469613.5:c.326C=
ENST00000478368.1:c.699C=	ENSP00000420647.1:p.Leu233=
NM_004656.3:c.2127C=	NP_004647.1:p.Leu709=
XM_011534149.1:c.2196C=	XP_011532451.1:p.Leu732=
XM_011534150.1:c.2151C=	XP_011532452.1:p.Leu717=
XM_011534151.1:c.2142C=	XP_011532453.1:p.Leu714=
XM_011534152.1:c.2082C=	XP_011532454.1:p.Leu694=
XM_011534149.3:c.2196C=	XP_011532451.1:p.Leu732=
XM_011534150.3:c.2151C=	XP_011532452.1:p.Leu717=
XM_011534151.3:c.2142C=	XP_011532453.1:p.Leu714=
XM_011534152.2:c.2082C=	XP_011532454.1:p.Leu694=
XM_017007303.2:c.2073C=	XP_016862792.1:p.Leu691=
NM_004656.4:c.2127C= MANE Select	NP_004647.1:p.Leu709=