Canonical Allele Identifier: CA1364834585

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402396C= , CM000665.2:g.52402396C=	GRCh38
NC_000003.11:g.52436412C= , CM000665.1:g.52436412C=	GRCh37
NC_000003.10:g.52411452C=	NCBI36
NG_031859.1:g.12598G= , LRG_529:g.12598G=
NG_052911.1:g.91078C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.2082G= MANE Select	ENSP00000417132.1:p.Gln694=
ENST00000296288.9:c.2028G=	ENSP00000296288.5:p.Gln676=
ENST00000460680.5:c.2082G=	ENSP00000417132.1:p.Gln694=
ENST00000466093.1:n.755G=
ENST00000469613.5:c.281G=
ENST00000478368.1:c.654G=	ENSP00000420647.1:p.Gln218=
NM_004656.3:c.2082G=	NP_004647.1:p.Gln694=
XM_011534149.1:c.2151G=	XP_011532451.1:p.Gln717=
XM_011534150.1:c.2106G=	XP_011532452.1:p.Gln702=
XM_011534151.1:c.2097G=	XP_011532453.1:p.Gln699=
XM_011534152.1:c.2037G=	XP_011532454.1:p.Gln679=
XM_011534149.3:c.2151G=	XP_011532451.1:p.Gln717=
XM_011534150.3:c.2106G=	XP_011532452.1:p.Gln702=
XM_011534151.3:c.2097G=	XP_011532453.1:p.Gln699=
XM_011534152.2:c.2037G=	XP_011532454.1:p.Gln679=
XM_017007303.2:c.2028G=	XP_016862792.1:p.Gln676=
NM_004656.4:c.2082G= MANE Select	NP_004647.1:p.Gln694=