Canonical Allele Identifier: CA645529872
Gene: BAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52402675_52402678del , CM000665.2:g.52402675_52402678del GRCh38
NC_000003.11:g.52436691_52436694del , CM000665.1:g.52436691_52436694del GRCh37
NC_000003.10:g.52411731_52411734del NCBI36
NG_031859.1:g.12317_12320del , LRG_529:g.12317_12320del

Transcript Alleles

HGVS Amino-acid Change
ENST00000460680.6:c.1984-3_1984del
ENST00000296288.9:c.1930-3_1930del
ENST00000460680.5:c.1984-3_1984del
ENST00000466093.1:n.657-3_657del
ENST00000469613.5:c.183-3_183del
ENST00000478368.1:c.556-3_556del
NM_004656.3:c.1984-3_1984del
XM_011534149.1:c.2053-3_2053del
XM_011534150.1:c.2008-3_2008del
XM_011534151.1:c.1999-3_1999del
XM_011534152.1:c.1939-3_1939del
XM_011534149.3:c.2053-3_2053del
XM_011534150.3:c.2008-3_2008del
XM_011534151.3:c.1999-3_1999del
XM_011534152.2:c.1939-3_1939del
XM_017007303.2:c.1930-3_1930del
NM_004656.4:c.1984-3_1984del