Canonical Allele Identifier: CA2666006819

Gene: BAP1

Linked Data

• gnomAD v4: 3-52402524-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402524G>T , CM000665.2:g.52402524G>T	GRCh38
NC_000003.11:g.52436540G>T , CM000665.1:g.52436540G>T	GRCh37
NC_000003.10:g.52411580G>T	NCBI36
NG_031859.1:g.12470C>A , LRG_529:g.12470C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.2056+78C>A MANE Select	ENSP00000417132.1:n.2056+78C>A
ENST00000296288.9:c.2002+78C>A	ENSP00000296288.5:n.2002+78C>A
ENST00000460680.5:c.2056+78C>A	ENSP00000417132.1:n.2056+78C>A
ENST00000466093.1:n.729+78C>A
ENST00000469613.5:c.255+78C>A
ENST00000478368.1:c.628+78C>A	ENSP00000420647.1:n.628+78C>A
NM_004656.3:c.2056+78C>A	NP_004647.1:n.2056+78C>A
XM_011534149.1:c.2125+78C>A	XP_011532451.1:n.2125+78C>A
XM_011534150.1:c.2080+78C>A	XP_011532452.1:n.2080+78C>A
XM_011534151.1:c.2071+78C>A	XP_011532453.1:n.2071+78C>A
XM_011534152.1:c.2011+78C>A	XP_011532454.1:n.2011+78C>A
XM_011534149.3:c.2125+78C>A	XP_011532451.1:n.2125+78C>A
XM_011534150.3:c.2080+78C>A	XP_011532452.1:n.2080+78C>A
XM_011534151.3:c.2071+78C>A	XP_011532453.1:n.2071+78C>A
XM_011534152.2:c.2011+78C>A	XP_011532454.1:n.2011+78C>A
XM_017007303.2:c.2002+78C>A	XP_016862792.1:n.2002+78C>A
NM_004656.4:c.2056+78C>A MANE Select	NP_004647.1:n.2056+78C>A