Canonical Allele Identifier: CA1364834555

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402378C= , CM000665.2:g.52402378C=	GRCh38
NC_000003.11:g.52436394C= , CM000665.1:g.52436394C=	GRCh37
NC_000003.10:g.52411434C=	NCBI36
NG_031859.1:g.12616G= , LRG_529:g.12616G=
NG_052911.1:g.91060C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2100G= MANE Select	ENSP00000417132.1:p.Arg700=
ENST00000296288.9:c.2046G=	ENSP00000296288.5:p.Arg682=
ENST00000460680.5:c.2100G=	ENSP00000417132.1:p.Arg700=
ENST00000466093.1:n.773G=
ENST00000469613.5:c.299G=
ENST00000478368.1:c.672G=	ENSP00000420647.1:p.Arg224=
NM_004656.3:c.2100G=	NP_004647.1:p.Arg700=
XM_011534149.1:c.2169G=	XP_011532451.1:p.Arg723=
XM_011534150.1:c.2124G=	XP_011532452.1:p.Arg708=
XM_011534151.1:c.2115G=	XP_011532453.1:p.Arg705=
XM_011534152.1:c.2055G=	XP_011532454.1:p.Arg685=
XM_011534149.3:c.2169G=	XP_011532451.1:p.Arg723=
XM_011534150.3:c.2124G=	XP_011532452.1:p.Arg708=
XM_011534151.3:c.2115G=	XP_011532453.1:p.Arg705=
XM_011534152.2:c.2055G=	XP_011532454.1:p.Arg685=
XM_017007303.2:c.2046G=	XP_016862792.1:p.Arg682=
NM_004656.4:c.2100G= MANE Select	NP_004647.1:p.Arg700=