Canonical Allele Identifier: CA913187447

Gene: BAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52405445C>T , CM000665.2:g.52405445C>T	GRCh38
NC_000003.11:g.52439461C>T , CM000665.1:g.52439461C>T	GRCh37
NC_000003.10:g.52414501C>T	NCBI36
NG_031859.1:g.9549G>A , LRG_529:g.9549G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004656.4:c.932-151G>A MANE Select	NP_004647.1:n.932-151G>A
ENST00000460680.6:c.932-151G>A MANE Select	ENSP00000417132.1:n.932-151G>A
NM_004656.3:c.932-151G>A	NP_004647.1:n.932-151G>A
ENST00000296288.9:c.878-151G>A	ENSP00000296288.5:n.878-151G>A
ENST00000460680.5:c.932-151G>A	ENSP00000417132.1:n.932-151G>A
ENST00000490804.1:n.209G>A
XM_011534149.1:c.932-151G>A	XP_011532451.1:n.932-151G>A
XM_011534149.3:c.932-151G>A	XP_011532451.1:n.932-151G>A
XM_011534150.1:c.932-151G>A	XP_011532452.1:n.932-151G>A
XM_011534150.3:c.932-151G>A	XP_011532452.1:n.932-151G>A
XM_011534151.1:c.878-151G>A	XP_011532453.1:n.878-151G>A
XM_011534151.3:c.878-151G>A	XP_011532453.1:n.878-151G>A
XM_011534152.1:c.932-151G>A	XP_011532454.1:n.932-151G>A
XM_011534152.2:c.932-151G>A	XP_011532454.1:n.932-151G>A
XM_017007303.2:c.878-151G>A	XP_016862792.1:n.878-151G>A