Canonical Allele Identifier: CA2756265849

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402997_52402998insACACA , CM000665.2:g.52402997_52402998insACACA	GRCh38
NC_000003.11:g.52437013_52437014insACACA , CM000665.1:g.52437013_52437014insACACA	GRCh37
NC_000003.10:g.52412053_52412054insACACA	NCBI36
NG_031859.1:g.11997_11998insGTGTT , LRG_529:g.11997_11998insGTGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1891-126_1891-125insGTGTT MANE Select	ENSP00000417132.1:n.1891-126_1891-125insGTGTT
ENST00000296288.9:c.1837-126_1837-125insGTGTT	ENSP00000296288.5:n.1837-126_1837-125insGTGTT
ENST00000460680.5:c.1891-126_1891-125insGTGTT	ENSP00000417132.1:n.1891-126_1891-125insGTGTT
ENST00000466093.1:n.438_439insGTGTT
ENST00000469613.5:c.120-156_120-155insGTGTT
ENST00000478368.1:c.394-57_394-56insGTGTT	ENSP00000420647.1:n.394-57_394-56insGTGTT
NM_004656.3:c.1891-126_1891-125insGTGTT	NP_004647.1:n.1891-126_1891-125insGTGTT
XM_011534149.1:c.1891-57_1891-56insGTGTT	XP_011532451.1:n.1891-57_1891-56insGTGTT
XM_011534150.1:c.1846-57_1846-56insGTGTT	XP_011532452.1:n.1846-57_1846-56insGTGTT
XM_011534151.1:c.1837-57_1837-56insGTGTT	XP_011532453.1:n.1837-57_1837-56insGTGTT
XM_011534152.1:c.1846-126_1846-125insGTGTT	XP_011532454.1:n.1846-126_1846-125insGTGTT
XM_011534149.3:c.1891-57_1891-56insGTGTT	XP_011532451.1:n.1891-57_1891-56insGTGTT
XM_011534150.3:c.1846-57_1846-56insGTGTT	XP_011532452.1:n.1846-57_1846-56insGTGTT
XM_011534151.3:c.1837-57_1837-56insGTGTT	XP_011532453.1:n.1837-57_1837-56insGTGTT
XM_011534152.2:c.1846-126_1846-125insGTGTT	XP_011532454.1:n.1846-126_1846-125insGTGTT
XM_017007303.2:c.1837-126_1837-125insGTGTT	XP_016862792.1:n.1837-126_1837-125insGTGTT
NM_004656.4:c.1891-126_1891-125insGTGTT MANE Select	NP_004647.1:n.1891-126_1891-125insGTGTT