Canonical Allele Identifier: CA2666006825

Gene: BAP1

Linked Data

• gnomAD v4: 3-52402525-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402525_52402526insT , CM000665.2:g.52402525_52402526insT	GRCh38
NC_000003.11:g.52436541_52436542insT , CM000665.1:g.52436541_52436542insT	GRCh37
NC_000003.10:g.52411581_52411582insT	NCBI36
NG_031859.1:g.12468_12469insA , LRG_529:g.12468_12469insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.2056+76_2056+77insA MANE Select	ENSP00000417132.1:n.2056+76_2056+77insA
ENST00000296288.9:c.2002+76_2002+77insA	ENSP00000296288.5:n.2002+76_2002+77insA
ENST00000460680.5:c.2056+76_2056+77insA	ENSP00000417132.1:n.2056+76_2056+77insA
ENST00000466093.1:n.729+76_729+77insA
ENST00000469613.5:c.255+76_255+77insA
ENST00000478368.1:c.628+76_628+77insA	ENSP00000420647.1:n.628+76_628+77insA
NM_004656.3:c.2056+76_2056+77insA	NP_004647.1:n.2056+76_2056+77insA
XM_011534149.1:c.2125+76_2125+77insA	XP_011532451.1:n.2125+76_2125+77insA
XM_011534150.1:c.2080+76_2080+77insA	XP_011532452.1:n.2080+76_2080+77insA
XM_011534151.1:c.2071+76_2071+77insA	XP_011532453.1:n.2071+76_2071+77insA
XM_011534152.1:c.2011+76_2011+77insA	XP_011532454.1:n.2011+76_2011+77insA
XM_011534149.3:c.2125+76_2125+77insA	XP_011532451.1:n.2125+76_2125+77insA
XM_011534150.3:c.2080+76_2080+77insA	XP_011532452.1:n.2080+76_2080+77insA
XM_011534151.3:c.2071+76_2071+77insA	XP_011532453.1:n.2071+76_2071+77insA
XM_011534152.2:c.2011+76_2011+77insA	XP_011532454.1:n.2011+76_2011+77insA
XM_017007303.2:c.2002+76_2002+77insA	XP_016862792.1:n.2002+76_2002+77insA
NM_004656.4:c.2056+76_2056+77insA MANE Select	NP_004647.1:n.2056+76_2056+77insA