Canonical Allele Identifier: CA1364836464

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52403490_52403491delinsTC , CM000665.2:g.52403490_52403491delinsTC	GRCh38
NC_000003.11:g.52437506_52437507delinsTC , CM000665.1:g.52437506_52437507delinsTC	GRCh37
NC_000003.10:g.52412546_52412547delinsTC	NCBI36
NG_031859.1:g.11503_11504delinsGA , LRG_529:g.11503_11504delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1654_1655delinsGA MANE Select	ENSP00000417132.1:p.Asp552=
ENST00000296288.9:c.1600_1601delinsGA	ENSP00000296288.5:p.Asp534=
ENST00000460680.5:c.1654_1655delinsGA	ENSP00000417132.1:p.Asp552=
ENST00000466093.1:n.61_62delinsGA
ENST00000469613.5:c.119+310_119+311delinsGA
ENST00000478368.1:c.157_158delinsGA	ENSP00000420647.1:p.Asp53=
NM_004656.3:c.1654_1655delinsGA	NP_004647.1:p.Asp552=
XM_011534149.1:c.1654_1655delinsGA	XP_011532451.1:p.Asp552=
XM_011534150.1:c.1654_1655delinsGA	XP_011532452.1:p.Asp552=
XM_011534151.1:c.1600_1601delinsGA	XP_011532453.1:p.Asp534=
XM_011534152.1:c.1654_1655delinsGA	XP_011532454.1:p.Asp552=
XM_011534149.3:c.1654_1655delinsGA	XP_011532451.1:p.Asp552=
XM_011534150.3:c.1654_1655delinsGA	XP_011532452.1:p.Asp552=
XM_011534151.3:c.1600_1601delinsGA	XP_011532453.1:p.Asp534=
XM_011534152.2:c.1654_1655delinsGA	XP_011532454.1:p.Asp552=
XM_017007303.2:c.1600_1601delinsGA	XP_016862792.1:p.Asp534=
NM_004656.4:c.1654_1655delinsGA MANE Select	NP_004647.1:p.Asp552=