Canonical Allele Identifier: CA645529917
Gene: BAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52403836_52403842del , CM000665.2:g.52403836_52403842del GRCh38
NC_000003.11:g.52437852_52437858del , CM000665.1:g.52437852_52437858del GRCh37
NC_000003.10:g.52412892_52412898del NCBI36
NG_031859.1:g.11152_11158del , LRG_529:g.11152_11158del

Transcript Alleles

HGVS Amino-acid Change
ENST00000460680.6:c.1303_1309del MANE Select ENSP00000417132.1:p.Gly435CysfsTer?
ENST00000296288.9:c.1249_1255del ENSP00000296288.5:p.Gly417CysfsTer?
ENST00000460680.5:c.1303_1309del ENSP00000417132.1:p.Gly435CysfsTer?
ENST00000469613.5:c.78_84del
ENST00000490804.1:n.731_737del
NM_004656.3:c.1303_1309del NP_004647.1:p.Gly435CysfsTer?
XM_011534149.1:c.1303_1309del XP_011532451.1:p.Gly435CysfsTer?
XM_011534150.1:c.1303_1309del XP_011532452.1:p.Gly435CysfsTer?
XM_011534151.1:c.1249_1255del XP_011532453.1:p.Gly417CysfsTer?
XM_011534152.1:c.1303_1309del XP_011532454.1:p.Gly435CysfsTer?
XM_011534149.3:c.1303_1309del XP_011532451.1:p.Gly435CysfsTer?
XM_011534150.3:c.1303_1309del XP_011532452.1:p.Gly435CysfsTer?
XM_011534151.3:c.1249_1255del XP_011532453.1:p.Gly417CysfsTer?
XM_011534152.2:c.1303_1309del XP_011532454.1:p.Gly435CysfsTer?
XM_017007303.2:c.1249_1255del XP_016862792.1:p.Gly417CysfsTer?
NM_004656.4:c.1303_1309del MANE Select NP_004647.1:p.Gly435CysfsTer?