Canonical Allele Identifier: CA1364834589

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402399C= , CM000665.2:g.52402399C=	GRCh38
NC_000003.11:g.52436415C= , CM000665.1:g.52436415C=	GRCh37
NC_000003.10:g.52411455C=	NCBI36
NG_031859.1:g.12595G= , LRG_529:g.12595G=
NG_052911.1:g.91081C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2079G= MANE Select	ENSP00000417132.1:p.Glu693=
ENST00000296288.9:c.2025G=	ENSP00000296288.5:p.Glu675=
ENST00000460680.5:c.2079G=	ENSP00000417132.1:p.Glu693=
ENST00000466093.1:n.752G=
ENST00000469613.5:c.278G=
ENST00000478368.1:c.651G=	ENSP00000420647.1:p.Glu217=
NM_004656.3:c.2079G=	NP_004647.1:p.Glu693=
XM_011534149.1:c.2148G=	XP_011532451.1:p.Glu716=
XM_011534150.1:c.2103G=	XP_011532452.1:p.Glu701=
XM_011534151.1:c.2094G=	XP_011532453.1:p.Glu698=
XM_011534152.1:c.2034G=	XP_011532454.1:p.Glu678=
XM_011534149.3:c.2148G=	XP_011532451.1:p.Glu716=
XM_011534150.3:c.2103G=	XP_011532452.1:p.Glu701=
XM_011534151.3:c.2094G=	XP_011532453.1:p.Glu698=
XM_011534152.2:c.2034G=	XP_011532454.1:p.Glu678=
XM_017007303.2:c.2025G=	XP_016862792.1:p.Glu675=
NM_004656.4:c.2079G= MANE Select	NP_004647.1:p.Glu693=