Canonical Allele Identifier: CA2639154643

Gene: BRIP1

Linked Data

• gnomAD v4: 17-61715853-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61715857del , CM000679.2:g.61715857del	GRCh38
NC_000017.10:g.59793218del , CM000679.1:g.59793218del	GRCh37
NC_000017.9:g.57148000del	NCBI36
NG_007409.2:g.152706del , LRG_300:g.152706del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682066.1:c.2622+97del	ENSP00000507191.1:n.2622+97del
ENST00000682073.1:n.1232+97del
ENST00000682433.1:n.1571+97del
ENST00000682453.1:c.2492+97del	ENSP00000506943.1:n.2492+97del
ENST00000682477.1:c.*1918+97del	ENSP00000507075.1:n.*1918+97del
ENST00000682589.1:n.8369+97del
ENST00000682755.1:c.2270+97del	ENSP00000507660.1:n.2270+97del
ENST00000682989.1:c.2492+97del	ENSP00000507786.1:n.2492+97del
ENST00000683039.1:c.2492+97del	ENSP00000508303.1:n.2492+97del
ENST00000683235.1:c.2492+97del	ENSP00000507646.1:n.2492+97del
ENST00000683535.1:n.622+97del
ENST00000684471.1:n.905+97del
ENST00000684584.1:c.1985+97del	ENSP00000508044.1:n.1985+97del
ENST00000684626.1:n.821+97del
ENST00000684769.1:c.557+97del	ENSP00000507691.1:n.557+97del
ENST00000259008.7:c.2492+97del MANE Select	ENSP00000259008.2:n.2492+97del
ENST00000259008.6:c.2492+97del	ENSP00000259008.2:n.2492+97del
ENST00000577598.5:c.2492+97del	ENSP00000464654.1:n.2492+97del
NM_032043.2:c.2492+97del , LRG_300t1:c.2492+97del	NP_114432.2:n.2492+97del
XM_011525332.1:c.2552+97del	XP_011523634.1:n.2552+97del
XM_011525333.1:c.2552+97del	XP_011523635.1:n.2552+97del
XM_011525334.1:c.2552+97del	XP_011523636.1:n.2552+97del
XM_011525335.1:c.2492+97del	XP_011523637.1:n.2492+97del
XM_011525336.1:c.2432+97del	XP_011523638.1:n.2432+97del
XM_011525337.1:c.2351+97del	XP_011523639.1:n.2351+97del
XM_011525338.1:c.2069+97del	XP_011523640.1:n.2069+97del
XM_011525340.1:c.2552+97del	XP_011523642.1:n.2552+97del
XM_011525332.3:c.2552+97del	XP_011523634.1:n.2552+97del
XM_011525333.3:c.2552+97del	XP_011523635.1:n.2552+97del
XM_011525334.2:c.2552+97del	XP_011523636.1:n.2552+97del
XM_011525335.3:c.2492+97del	XP_011523637.1:n.2492+97del
XM_011525336.2:c.2432+97del	XP_011523638.1:n.2432+97del
XM_011525337.2:c.2351+97del	XP_011523639.1:n.2351+97del
XM_011525338.2:c.2069+97del	XP_011523640.1:n.2069+97del
XM_011525340.3:c.2552+97del	XP_011523642.1:n.2552+97del
XM_017025200.1:c.2009+97del	XP_016880689.1:n.2009+97del
XM_017025201.1:c.2009+97del	XP_016880690.1:n.2009+97del
XM_017025202.1:c.638+97del	XP_016880691.1:n.638+97del
XM_017025203.1:c.638+97del	XP_016880692.1:n.638+97del
NM_032043.3:c.2492+97del MANE Select	NP_114432.2:n.2492+97del