Canonical Allele Identifier: CA2269199715

Gene: BRIP1

Linked Data

• dbSNP Id: rs2078793702

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61850045_61850048del , CM000679.2:g.61850045_61850048del	GRCh38
NC_000017.10:g.59927406_59927409del , CM000679.1:g.59927406_59927409del	GRCh37
NC_000017.9:g.57282188_57282191del	NCBI36
NG_007409.2:g.18515_18518del , LRG_300:g.18515_18518del

Transcript Alleles

HGVS	Amino-acid change
ENST00000577913.2:c.380-789_380-786del	ENSP00000462274.2:n.380-789_380-786del
ENST00000584322.2:c.380-789_380-786del	ENSP00000463272.2:n.380-789_380-786del
ENST00000682369.1:c.380-789_380-786del	ENSP00000507450.1:n.380-789_380-786del
ENST00000682453.1:c.380-789_380-786del	ENSP00000506943.1:n.380-789_380-786del
ENST00000682477.1:c.380-789_380-786del	ENSP00000507075.1:n.380-789_380-786del
ENST00000682589.1:n.2121-789_2121-786del
ENST00000682755.1:c.380-789_380-786del	ENSP00000507660.1:n.380-789_380-786del
ENST00000682989.1:c.380-789_380-786del	ENSP00000507786.1:n.380-789_380-786del
ENST00000683039.1:c.380-789_380-786del	ENSP00000508303.1:n.380-789_380-786del
ENST00000683235.1:c.380-789_380-786del	ENSP00000507646.1:n.380-789_380-786del
ENST00000683381.1:c.380-789_380-786del	ENSP00000508184.1:n.380-789_380-786del
ENST00000683672.1:c.83-2825_83-2822del	ENSP00000506781.1:n.83-2825_83-2822del
ENST00000259008.7:c.380-789_380-786del MANE Select	ENSP00000259008.2:n.380-789_380-786del
ENST00000259008.6:c.380-789_380-786del	ENSP00000259008.2:n.380-789_380-786del
ENST00000577598.5:c.380-789_380-786del	ENSP00000464654.1:n.380-789_380-786del
NM_032043.2:c.380-789_380-786del , LRG_300t1:c.380-789_380-786del	NP_114432.2:n.380-789_380-786del
XM_011525332.1:c.380-789_380-786del	XP_011523634.1:n.380-789_380-786del
XM_011525333.1:c.380-789_380-786del	XP_011523635.1:n.380-789_380-786del
XM_011525334.1:c.380-789_380-786del	XP_011523636.1:n.380-789_380-786del
XM_011525335.1:c.380-789_380-786del	XP_011523637.1:n.380-789_380-786del
XM_011525336.1:c.380-789_380-786del	XP_011523638.1:n.380-789_380-786del
XM_011525337.1:c.380-789_380-786del	XP_011523639.1:n.380-789_380-786del
XM_011525338.1:c.25-2825_25-2822del	XP_011523640.1:n.25-2825_25-2822del
XM_011525339.1:c.380-789_380-786del	XP_011523641.1:n.380-789_380-786del
XM_011525340.1:c.380-789_380-786del	XP_011523642.1:n.380-789_380-786del
XM_011525341.1:c.380-789_380-786del	XP_011523643.1:n.380-789_380-786del
XM_011525332.3:c.380-789_380-786del	XP_011523634.1:n.380-789_380-786del
XM_011525333.3:c.380-789_380-786del	XP_011523635.1:n.380-789_380-786del
XM_011525334.2:c.380-789_380-786del	XP_011523636.1:n.380-789_380-786del
XM_011525335.3:c.380-789_380-786del	XP_011523637.1:n.380-789_380-786del
XM_011525336.2:c.380-789_380-786del	XP_011523638.1:n.380-789_380-786del
XM_011525337.2:c.380-789_380-786del	XP_011523639.1:n.380-789_380-786del
XM_011525338.2:c.25-2825_25-2822del	XP_011523640.1:n.25-2825_25-2822del
XM_011525339.3:c.380-789_380-786del	XP_011523641.1:n.380-789_380-786del
XM_011525340.3:c.380-789_380-786del	XP_011523642.1:n.380-789_380-786del
XM_011525341.3:c.380-789_380-786del	XP_011523643.1:n.380-789_380-786del
XM_017025200.1:c.25-2825_25-2822del	XP_016880689.1:n.25-2825_25-2822del
NM_032043.3:c.380-789_380-786del MANE Select	NP_114432.2:n.380-789_380-786del