Canonical Allele Identifier: CA2666006677
Gene: BAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52402451_52402471del , CM000665.2:g.52402451_52402471del GRCh38
NC_000003.11:g.52436467_52436487del , CM000665.1:g.52436467_52436487del GRCh37
NC_000003.10:g.52411507_52411527del NCBI36
NG_031859.1:g.12527_12547del , LRG_529:g.12527_12547del
NG_052911.1:g.91133_91153del

Transcript Alleles

HGVS Amino-acid change
ENST00000460680.6:c.2057-46_2057-26del MANE Select ENSP00000417132.1:n.2057-46_2057-26del
ENST00000296288.9:c.2003-46_2003-26del ENSP00000296288.5:n.2003-46_2003-26del
ENST00000460680.5:c.2057-46_2057-26del ENSP00000417132.1:n.2057-46_2057-26del
ENST00000466093.1:n.730-46_730-26del
ENST00000469613.5:c.256-46_256-26del
ENST00000478368.1:c.629-46_629-26del ENSP00000420647.1:n.629-46_629-26del
NM_004656.3:c.2057-46_2057-26del NP_004647.1:n.2057-46_2057-26del
XM_011534149.1:c.2126-46_2126-26del XP_011532451.1:n.2126-46_2126-26del
XM_011534150.1:c.2081-46_2081-26del XP_011532452.1:n.2081-46_2081-26del
XM_011534151.1:c.2072-46_2072-26del XP_011532453.1:n.2072-46_2072-26del
XM_011534152.1:c.2012-46_2012-26del XP_011532454.1:n.2012-46_2012-26del
XM_011534149.3:c.2126-46_2126-26del XP_011532451.1:n.2126-46_2126-26del
XM_011534150.3:c.2081-46_2081-26del XP_011532452.1:n.2081-46_2081-26del
XM_011534151.3:c.2072-46_2072-26del XP_011532453.1:n.2072-46_2072-26del
XM_011534152.2:c.2012-46_2012-26del XP_011532454.1:n.2012-46_2012-26del
XM_017007303.2:c.2003-46_2003-26del XP_016862792.1:n.2003-46_2003-26del
NM_004656.4:c.2057-46_2057-26del MANE Select NP_004647.1:n.2057-46_2057-26del