Canonical Allele Identifier: CA915950697

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 821357
• ClinVar RCV Id: RCV001015693
• dbSNP Id: rs1603293314

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61715951del , CM000679.2:g.61715951del	GRCh38
NC_000017.10:g.59793312del , CM000679.1:g.59793312del	GRCh37
NC_000017.9:g.57148094del	NCBI36
NG_007409.2:g.152610del , LRG_300:g.152610del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682066.1:c.2622+1del
ENST00000682073.1:n.1232+1del
ENST00000682433.1:n.1571+1del
ENST00000682453.1:c.2492+1del
ENST00000682477.1:c.*1918+1del
ENST00000682589.1:n.8369+1del
ENST00000682755.1:c.2270+1del
ENST00000682989.1:c.2492+1del
ENST00000683039.1:c.2492+1del
ENST00000683235.1:c.2492+1del
ENST00000683535.1:n.622+1del
ENST00000684471.1:n.905+1del
ENST00000684584.1:c.1985+1del
ENST00000684626.1:n.821+1del
ENST00000684769.1:c.557+1del
ENST00000259008.7:c.2492+1del
ENST00000259008.6:c.2492+1del
ENST00000577598.5:c.2492+1del
NM_032043.2:c.2492+1del , LRG_300t1:c.2492+1del
XM_011525332.1:c.2552+1del
XM_011525333.1:c.2552+1del
XM_011525334.1:c.2552+1del
XM_011525335.1:c.2492+1del
XM_011525336.1:c.2432+1del
XM_011525337.1:c.2351+1del
XM_011525338.1:c.2069+1del
XM_011525340.1:c.2552+1del
XM_011525332.3:c.2552+1del
XM_011525333.3:c.2552+1del
XM_011525334.2:c.2552+1del
XM_011525335.3:c.2492+1del
XM_011525336.2:c.2432+1del
XM_011525337.2:c.2351+1del
XM_011525338.2:c.2069+1del
XM_011525340.3:c.2552+1del
XM_017025200.1:c.2009+1del
XM_017025201.1:c.2009+1del
XM_017025202.1:c.638+1del
XM_017025203.1:c.638+1del
NM_032043.3:c.2492+1del