Canonical Allele Identifier: CA2666006679

Gene: BAP1

Linked Data

• gnomAD v4: 3-52402448-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52402448A>T , CM000665.2:g.52402448A>T	GRCh38
NC_000003.11:g.52436464A>T , CM000665.1:g.52436464A>T	GRCh37
NC_000003.10:g.52411504A>T	NCBI36
NG_031859.1:g.12546T>A , LRG_529:g.12546T>A
NG_052911.1:g.91130A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000460680.6:c.2057-27T>A MANE Select	ENSP00000417132.1:n.2057-27T>A
ENST00000296288.9:c.2003-27T>A	ENSP00000296288.5:n.2003-27T>A
ENST00000460680.5:c.2057-27T>A	ENSP00000417132.1:n.2057-27T>A
ENST00000466093.1:n.730-27T>A
ENST00000469613.5:c.256-27T>A
ENST00000478368.1:c.629-27T>A	ENSP00000420647.1:n.629-27T>A
NM_004656.3:c.2057-27T>A	NP_004647.1:n.2057-27T>A
XM_011534149.1:c.2126-27T>A	XP_011532451.1:n.2126-27T>A
XM_011534150.1:c.2081-27T>A	XP_011532452.1:n.2081-27T>A
XM_011534151.1:c.2072-27T>A	XP_011532453.1:n.2072-27T>A
XM_011534152.1:c.2012-27T>A	XP_011532454.1:n.2012-27T>A
XM_011534149.3:c.2126-27T>A	XP_011532451.1:n.2126-27T>A
XM_011534150.3:c.2081-27T>A	XP_011532452.1:n.2081-27T>A
XM_011534151.3:c.2072-27T>A	XP_011532453.1:n.2072-27T>A
XM_011534152.2:c.2012-27T>A	XP_011532454.1:n.2012-27T>A
XM_017007303.2:c.2003-27T>A	XP_016862792.1:n.2003-27T>A
NM_004656.4:c.2057-27T>A MANE Select	NP_004647.1:n.2057-27T>A