Canonical Allele Identifier: CA2756265840
Gene: BAP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52402972_52402973insGTTCAGAAGAGGCAGACTTTGTCCCTTTCATGGTCAATGCACGGTCTATGTCCAGAGGATTGATACTACCATAGCAATTAGTAATATCAGAGACAAACA , CM000665.2:g.52402972_52402973insGTTCAGAAGAGGCAGACTTTGTCCCTTTCATGGTCAATGCACGGTCTATGTCCAGAGGATTGATACTACCATAGCAATTAGTAATATCAGAGACAAACA GRCh38
NC_000003.11:g.52436988_52436989insGTTCAGAAGAGGCAGACTTTGTCCCTTTCATGGTCAATGCACGGTCTATGTCCAGAGGATTGATACTACCATAGCAATTAGTAATATCAGAGACAAACA , CM000665.1:g.52436988_52436989insGTTCAGAAGAGGCAGACTTTGTCCCTTTCATGGTCAATGCACGGTCTATGTCCAGAGGATTGATACTACCATAGCAATTAGTAATATCAGAGACAAACA GRCh37
NC_000003.10:g.52412028_52412029insGTTCAGAAGAGGCAGACTTTGTCCCTTTCATGGTCAATGCACGGTCTATGTCCAGAGGATTGATACTACCATAGCAATTAGTAATATCAGAGACAAACA NCBI36
NG_031859.1:g.12021_12022insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC , LRG_529:g.12021_12022insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000460680.6:c.1891-102_1891-101insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC MANE Select ENSP00000417132.1:n.1891-102_1891-101insTGTTTGTCTCTGATATTACTA...
ENST00000296288.9:c.1837-102_1837-101insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC ENSP00000296288.5:n.1837-102_1837-101insTGTTTGTCTCTGATATTACTA...
ENST00000460680.5:c.1891-102_1891-101insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC ENSP00000417132.1:n.1891-102_1891-101insTGTTTGTCTCTGATATTACTA...
ENST00000466093.1:n.462_463insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC
ENST00000469613.5:c.120-132_120-131insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC
ENST00000478368.1:c.394-33_394-32insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC ENSP00000420647.1:n.394-33_394-32insTGTTTGTCTCTGATATTACTAATTG...
NM_004656.3:c.1891-102_1891-101insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC NP_004647.1:n.1891-102_1891-101insTGTTTGTCTCTGATATTACTAATTGCT...
XM_011534149.1:c.1891-33_1891-32insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC XP_011532451.1:n.1891-33_1891-32insTGTTTGTCTCTGATATTACTAATTGC...
XM_011534150.1:c.1846-33_1846-32insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC XP_011532452.1:n.1846-33_1846-32insTGTTTGTCTCTGATATTACTAATTGC...
XM_011534151.1:c.1837-33_1837-32insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC XP_011532453.1:n.1837-33_1837-32insTGTTTGTCTCTGATATTACTAATTGC...
XM_011534152.1:c.1846-102_1846-101insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC XP_011532454.1:n.1846-102_1846-101insTGTTTGTCTCTGATATTACTAATT...
XM_011534149.3:c.1891-33_1891-32insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC XP_011532451.1:n.1891-33_1891-32insTGTTTGTCTCTGATATTACTAATTGC...
XM_011534150.3:c.1846-33_1846-32insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC XP_011532452.1:n.1846-33_1846-32insTGTTTGTCTCTGATATTACTAATTGC...
XM_011534151.3:c.1837-33_1837-32insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC XP_011532453.1:n.1837-33_1837-32insTGTTTGTCTCTGATATTACTAATTGC...
XM_011534152.2:c.1846-102_1846-101insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC XP_011532454.1:n.1846-102_1846-101insTGTTTGTCTCTGATATTACTAATT...
XM_017007303.2:c.1837-102_1837-101insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC XP_016862792.1:n.1837-102_1837-101insTGTTTGTCTCTGATATTACTAATT...
NM_004656.4:c.1891-102_1891-101insTGTTTGTCTCTGATATTACTAATTGCTATGGTAGTATCAATCCTCTGGACATAGACCGTGCATTGACCATGAAAGGGACAAAGTCTGCCTCTTCTGAAC MANE Select NP_004647.1:n.1891-102_1891-101insTGTTTGTCTCTGATATTACTAATTGCT...