Canonical Allele Identifier: CA1364835947

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403266G= , CM000665.2:g.52403266G=	GRCh38
NC_000003.11:g.52437282G= , CM000665.1:g.52437282G=	GRCh37
NC_000003.10:g.52412322G=	NCBI36
NG_031859.1:g.11728C= , LRG_529:g.11728C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1762C= MANE Select	ENSP00000417132.1:p.Pro588=
ENST00000296288.9:c.1708C=	ENSP00000296288.5:p.Pro570=
ENST00000460680.5:c.1762C=	ENSP00000417132.1:p.Pro588=
ENST00000466093.1:n.169C=
ENST00000469613.5:c.120-425C=
ENST00000478368.1:c.265C=	ENSP00000420647.1:p.Pro89=
NM_004656.3:c.1762C=	NP_004647.1:p.Pro588=
XM_011534149.1:c.1762C=	XP_011532451.1:p.Pro588=
XM_011534150.1:c.1762C=	XP_011532452.1:p.Pro588=
XM_011534151.1:c.1708C=	XP_011532453.1:p.Pro570=
XM_011534152.1:c.1762C=	XP_011532454.1:p.Pro588=
XM_011534149.3:c.1762C=	XP_011532451.1:p.Pro588=
XM_011534150.3:c.1762C=	XP_011532452.1:p.Pro588=
XM_011534151.3:c.1708C=	XP_011532453.1:p.Pro570=
XM_011534152.2:c.1762C=	XP_011532454.1:p.Pro588=
XM_017007303.2:c.1708C=	XP_016862792.1:p.Pro570=
NM_004656.4:c.1762C= MANE Select	NP_004647.1:p.Pro588=