Canonical Allele Identifier: CA2269179435

Gene: BRIP1

Linked Data

• dbSNP Id: rs2077982310

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61801105_61801109del , CM000679.2:g.61801105_61801109del	GRCh38
NC_000017.10:g.59878466_59878470del , CM000679.1:g.59878466_59878470del	GRCh37
NC_000017.9:g.57233248_57233252del	NCBI36
NG_007409.2:g.67453_67457del , LRG_300:g.67453_67457del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.633+146_633+150del	ENSP00000463827.2:n.633+146_633+150del
ENST00000584322.2:c.1140+146_1140+150del	ENSP00000463272.2:n.1140+146_1140+150del
ENST00000682066.1:c.633+146_633+150del	ENSP00000507191.1:n.633+146_633+150del
ENST00000682453.1:c.1140+146_1140+150del	ENSP00000506943.1:n.1140+146_1140+150del
ENST00000682477.1:c.1140+146_1140+150del	ENSP00000507075.1:n.1140+146_1140+150del
ENST00000682589.1:n.2881+146_2881+150del
ENST00000682611.1:c.633+146_633+150del	ENSP00000508326.1:n.633+146_633+150del
ENST00000682755.1:c.919-1808_919-1804del	ENSP00000507660.1:n.919-1808_919-1804del
ENST00000682989.1:c.1140+146_1140+150del	ENSP00000507786.1:n.1140+146_1140+150del
ENST00000683039.1:c.1140+146_1140+150del	ENSP00000508303.1:n.1140+146_1140+150del
ENST00000683235.1:c.1140+146_1140+150del	ENSP00000507646.1:n.1140+146_1140+150del
ENST00000683381.1:c.1140+146_1140+150del	ENSP00000508184.1:n.1140+146_1140+150del
ENST00000683692.1:c.718+146_718+150del	ENSP00000507964.1:n.718+146_718+150del
ENST00000684584.1:c.633+146_633+150del	ENSP00000508044.1:n.633+146_633+150del
ENST00000259008.7:c.1140+146_1140+150del MANE Select	ENSP00000259008.2:n.1140+146_1140+150del
ENST00000259008.6:c.1140+146_1140+150del	ENSP00000259008.2:n.1140+146_1140+150del
ENST00000577598.5:c.1140+146_1140+150del	ENSP00000464654.1:n.1140+146_1140+150del
NM_032043.2:c.1140+146_1140+150del , LRG_300t1:c.1140+146_1140+150del	NP_114432.2:n.1140+146_1140+150del
XM_011525332.1:c.1140+146_1140+150del	XP_011523634.1:n.1140+146_1140+150del
XM_011525333.1:c.1140+146_1140+150del	XP_011523635.1:n.1140+146_1140+150del
XM_011525334.1:c.1140+146_1140+150del	XP_011523636.1:n.1140+146_1140+150del
XM_011525335.1:c.1140+146_1140+150del	XP_011523637.1:n.1140+146_1140+150del
XM_011525336.1:c.1140+146_1140+150del	XP_011523638.1:n.1140+146_1140+150del
XM_011525337.1:c.1140+146_1140+150del	XP_011523639.1:n.1140+146_1140+150del
XM_011525338.1:c.657+146_657+150del	XP_011523640.1:n.657+146_657+150del
XM_011525339.1:c.1140+146_1140+150del	XP_011523641.1:n.1140+146_1140+150del
XM_011525340.1:c.1140+146_1140+150del	XP_011523642.1:n.1140+146_1140+150del
XM_011525341.1:c.1140+146_1140+150del	XP_011523643.1:n.1140+146_1140+150del
XM_011525332.3:c.1140+146_1140+150del	XP_011523634.1:n.1140+146_1140+150del
XM_011525333.3:c.1140+146_1140+150del	XP_011523635.1:n.1140+146_1140+150del
XM_011525334.2:c.1140+146_1140+150del	XP_011523636.1:n.1140+146_1140+150del
XM_011525335.3:c.1140+146_1140+150del	XP_011523637.1:n.1140+146_1140+150del
XM_011525336.2:c.1140+146_1140+150del	XP_011523638.1:n.1140+146_1140+150del
XM_011525337.2:c.1140+146_1140+150del	XP_011523639.1:n.1140+146_1140+150del
XM_011525338.2:c.657+146_657+150del	XP_011523640.1:n.657+146_657+150del
XM_011525339.3:c.1140+146_1140+150del	XP_011523641.1:n.1140+146_1140+150del
XM_011525340.3:c.1140+146_1140+150del	XP_011523642.1:n.1140+146_1140+150del
XM_011525341.3:c.1140+146_1140+150del	XP_011523643.1:n.1140+146_1140+150del
XM_017025200.1:c.657+146_657+150del	XP_016880689.1:n.657+146_657+150del
XM_017025201.1:c.597+146_597+150del	XP_016880690.1:n.597+146_597+150del
NM_032043.3:c.1140+146_1140+150del MANE Select	NP_114432.2:n.1140+146_1140+150del