Canonical Allele Identifier: CA1364836382

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403439A= , CM000665.2:g.52403439A=	GRCh38
NC_000003.11:g.52437455A= , CM000665.1:g.52437455A=	GRCh37
NC_000003.10:g.52412495A=	NCBI36
NG_031859.1:g.11555T= , LRG_529:g.11555T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1706T= MANE Select	ENSP00000417132.1:p.Val569=
ENST00000296288.9:c.1652T=	ENSP00000296288.5:p.Val551=
ENST00000460680.5:c.1706T=	ENSP00000417132.1:p.Val569=
ENST00000466093.1:n.113T=
ENST00000469613.5:c.119+362T=
ENST00000478368.1:c.209T=	ENSP00000420647.1:p.Val70=
NM_004656.3:c.1706T=	NP_004647.1:p.Val569=
XM_011534149.1:c.1706T=	XP_011532451.1:p.Val569=
XM_011534150.1:c.1706T=	XP_011532452.1:p.Val569=
XM_011534151.1:c.1652T=	XP_011532453.1:p.Val551=
XM_011534152.1:c.1706T=	XP_011532454.1:p.Val569=
XM_011534149.3:c.1706T=	XP_011532451.1:p.Val569=
XM_011534150.3:c.1706T=	XP_011532452.1:p.Val569=
XM_011534151.3:c.1652T=	XP_011532453.1:p.Val551=
XM_011534152.2:c.1706T=	XP_011532454.1:p.Val569=
XM_017007303.2:c.1652T=	XP_016862792.1:p.Val551=
NM_004656.4:c.1706T= MANE Select	NP_004647.1:p.Val569=