Canonical Allele Identifier: CA645529898
Gene: BAP1 HGNC NCBI

Linked Data

COSMIC: COSM238941

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52403296_52403307del , CM000665.2:g.52403296_52403307del GRCh38
NC_000003.11:g.52437312_52437323del , CM000665.1:g.52437312_52437323del GRCh37
NC_000003.10:g.52412352_52412363del NCBI36
NG_031859.1:g.11687_11698del , LRG_529:g.11687_11698del

Transcript Alleles

HGVS Amino-acid Change
ENST00000460680.6:c.1730-9_1732del
ENST00000296288.9:c.1676-9_1678del
ENST00000460680.5:c.1730-9_1732del
ENST00000466093.1:n.137-9_139del
ENST00000469613.5:c.120-466_120-455del
ENST00000478368.1:c.233-9_235del
NM_004656.3:c.1730-9_1732del
XM_011534149.1:c.1730-9_1732del
XM_011534150.1:c.1730-9_1732del
XM_011534151.1:c.1676-9_1678del
XM_011534152.1:c.1730-9_1732del
XM_011534149.3:c.1730-9_1732del
XM_011534150.3:c.1730-9_1732del
XM_011534151.3:c.1676-9_1678del
XM_011534152.2:c.1730-9_1732del
XM_017007303.2:c.1676-9_1678del
NM_004656.4:c.1730-9_1732del