Canonical Allele Identifier: CA1364835425

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402958_52402959delinsCA , CM000665.2:g.52402958_52402959delinsCA	GRCh38
NC_000003.11:g.52436974_52436975delinsCA , CM000665.1:g.52436974_52436975delinsCA	GRCh37
NC_000003.10:g.52412014_52412015delinsCA	NCBI36
NG_031859.1:g.12035_12036delinsTG , LRG_529:g.12035_12036delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000460680.6:c.1891-88_1891-87delinsTG MANE Select	ENSP00000417132.1:n.1891-88_1891-87delinsTG
ENST00000296288.9:c.1837-88_1837-87delinsTG	ENSP00000296288.5:n.1837-88_1837-87delinsTG
ENST00000460680.5:c.1891-88_1891-87delinsTG	ENSP00000417132.1:n.1891-88_1891-87delinsTG
ENST00000466093.1:n.476_477delinsTG
ENST00000469613.5:c.120-118_120-117delinsTG
ENST00000478368.1:c.394-19_394-18delinsTG	ENSP00000420647.1:n.394-19_394-18delinsTG
NM_004656.3:c.1891-88_1891-87delinsTG	NP_004647.1:n.1891-88_1891-87delinsTG
XM_011534149.1:c.1891-19_1891-18delinsTG	XP_011532451.1:n.1891-19_1891-18delinsTG
XM_011534150.1:c.1846-19_1846-18delinsTG	XP_011532452.1:n.1846-19_1846-18delinsTG
XM_011534151.1:c.1837-19_1837-18delinsTG	XP_011532453.1:n.1837-19_1837-18delinsTG
XM_011534152.1:c.1846-88_1846-87delinsTG	XP_011532454.1:n.1846-88_1846-87delinsTG
XM_011534149.3:c.1891-19_1891-18delinsTG	XP_011532451.1:n.1891-19_1891-18delinsTG
XM_011534150.3:c.1846-19_1846-18delinsTG	XP_011532452.1:n.1846-19_1846-18delinsTG
XM_011534151.3:c.1837-19_1837-18delinsTG	XP_011532453.1:n.1837-19_1837-18delinsTG
XM_011534152.2:c.1846-88_1846-87delinsTG	XP_011532454.1:n.1846-88_1846-87delinsTG
XM_017007303.2:c.1837-88_1837-87delinsTG	XP_016862792.1:n.1837-88_1837-87delinsTG
NM_004656.4:c.1891-88_1891-87delinsTG MANE Select	NP_004647.1:n.1891-88_1891-87delinsTG