Canonical Allele Identifier: CA645529870
Gene: BAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52402661del , CM000665.2:g.52402661del GRCh38
NC_000003.11:g.52436677del , CM000665.1:g.52436677del GRCh37
NC_000003.10:g.52411717del NCBI36
NG_031859.1:g.12333del , LRG_529:g.12333del

Transcript Alleles

HGVS Amino-acid Change
ENST00000460680.6:c.1997del MANE Select ENSP00000417132.1:p.Arg666LysfsTer26
ENST00000296288.9:c.1943del ENSP00000296288.5:p.Arg648LysfsTer26
ENST00000460680.5:c.1997del ENSP00000417132.1:p.Arg666LysfsTer26
ENST00000466093.1:n.670del
ENST00000469613.5:c.196del
ENST00000478368.1:c.569del ENSP00000420647.1:p.Arg190LysfsTer26
NM_004656.3:c.1997del NP_004647.1:p.Arg666LysfsTer26
XM_011534149.1:c.2066del XP_011532451.1:p.Arg689LysfsTer26
XM_011534150.1:c.2021del XP_011532452.1:p.Arg674LysfsTer26
XM_011534151.1:c.2012del XP_011532453.1:p.Arg671LysfsTer26
XM_011534152.1:c.1952del XP_011532454.1:p.Arg651LysfsTer26
XM_011534149.3:c.2066del XP_011532451.1:p.Arg689LysfsTer26
XM_011534150.3:c.2021del XP_011532452.1:p.Arg674LysfsTer26
XM_011534151.3:c.2012del XP_011532453.1:p.Arg671LysfsTer26
XM_011534152.2:c.1952del XP_011532454.1:p.Arg651LysfsTer26
XM_017007303.2:c.1943del XP_016862792.1:p.Arg648LysfsTer26
NM_004656.4:c.1997del MANE Select NP_004647.1:p.Arg666LysfsTer26