Canonical Allele Identifier: CA645529886
Gene: BAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52403140_52403300del , CM000665.2:g.52403140_52403300del GRCh38
NC_000003.11:g.52437156_52437316del , CM000665.1:g.52437156_52437316del GRCh37
NC_000003.10:g.52412196_52412356del NCBI36
NG_031859.1:g.11696_11856del , LRG_529:g.11696_11856del

Transcript Alleles

HGVS Amino-acid change
ENST00000460680.6:c.1730_1890del
ENST00000296288.9:c.1676_1836del
ENST00000460680.5:c.1730_1890del
ENST00000466093.1:n.137_297del
ENST00000469613.5:c.120-457_120-297del
ENST00000478368.1:c.233_393del
NM_004656.3:c.1730_1890del
XM_011534149.1:c.1730_1890del
XM_011534150.1:c.1730_1845+45del
XM_011534151.1:c.1676_1836del
XM_011534152.1:c.1730_1845+45del
XM_011534149.3:c.1730_1890del
XM_011534150.3:c.1730_1845+45del
XM_011534151.3:c.1676_1836del
XM_011534152.2:c.1730_1845+45del
XM_017007303.2:c.1676_1836del
NM_004656.4:c.1730_1890del