Canonical Allele Identifier: CA2639156707

Gene: BRIP1

Linked Data

• gnomAD v4: 17-61801165-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61801165_61801166insG , CM000679.2:g.61801165_61801166insG	GRCh38
NC_000017.10:g.59878526_59878527insG , CM000679.1:g.59878526_59878527insG	GRCh37
NC_000017.9:g.57233308_57233309insG	NCBI36
NG_007409.2:g.67394_67395insC , LRG_300:g.67394_67395insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.633+87_633+88insC	ENSP00000463827.2:n.633+87_633+88insC
ENST00000584322.2:c.1140+87_1140+88insC	ENSP00000463272.2:n.1140+87_1140+88insC
ENST00000682066.1:c.633+87_633+88insC	ENSP00000507191.1:n.633+87_633+88insC
ENST00000682453.1:c.1140+87_1140+88insC	ENSP00000506943.1:n.1140+87_1140+88insC
ENST00000682477.1:c.1140+87_1140+88insC	ENSP00000507075.1:n.1140+87_1140+88insC
ENST00000682589.1:n.2881+87_2881+88insC
ENST00000682611.1:c.633+87_633+88insC	ENSP00000508326.1:n.633+87_633+88insC
ENST00000682755.1:c.919-1867_919-1866insC	ENSP00000507660.1:n.919-1867_919-1866insC
ENST00000682989.1:c.1140+87_1140+88insC	ENSP00000507786.1:n.1140+87_1140+88insC
ENST00000683039.1:c.1140+87_1140+88insC	ENSP00000508303.1:n.1140+87_1140+88insC
ENST00000683235.1:c.1140+87_1140+88insC	ENSP00000507646.1:n.1140+87_1140+88insC
ENST00000683381.1:c.1140+87_1140+88insC	ENSP00000508184.1:n.1140+87_1140+88insC
ENST00000683692.1:c.718+87_718+88insC	ENSP00000507964.1:n.718+87_718+88insC
ENST00000684584.1:c.633+87_633+88insC	ENSP00000508044.1:n.633+87_633+88insC
ENST00000259008.7:c.1140+87_1140+88insC MANE Select	ENSP00000259008.2:n.1140+87_1140+88insC
ENST00000259008.6:c.1140+87_1140+88insC	ENSP00000259008.2:n.1140+87_1140+88insC
ENST00000577598.5:c.1140+87_1140+88insC	ENSP00000464654.1:n.1140+87_1140+88insC
NM_032043.2:c.1140+87_1140+88insC , LRG_300t1:c.1140+87_1140+88insC	NP_114432.2:n.1140+87_1140+88insC
XM_011525332.1:c.1140+87_1140+88insC	XP_011523634.1:n.1140+87_1140+88insC
XM_011525333.1:c.1140+87_1140+88insC	XP_011523635.1:n.1140+87_1140+88insC
XM_011525334.1:c.1140+87_1140+88insC	XP_011523636.1:n.1140+87_1140+88insC
XM_011525335.1:c.1140+87_1140+88insC	XP_011523637.1:n.1140+87_1140+88insC
XM_011525336.1:c.1140+87_1140+88insC	XP_011523638.1:n.1140+87_1140+88insC
XM_011525337.1:c.1140+87_1140+88insC	XP_011523639.1:n.1140+87_1140+88insC
XM_011525338.1:c.657+87_657+88insC	XP_011523640.1:n.657+87_657+88insC
XM_011525339.1:c.1140+87_1140+88insC	XP_011523641.1:n.1140+87_1140+88insC
XM_011525340.1:c.1140+87_1140+88insC	XP_011523642.1:n.1140+87_1140+88insC
XM_011525341.1:c.1140+87_1140+88insC	XP_011523643.1:n.1140+87_1140+88insC
XM_011525332.3:c.1140+87_1140+88insC	XP_011523634.1:n.1140+87_1140+88insC
XM_011525333.3:c.1140+87_1140+88insC	XP_011523635.1:n.1140+87_1140+88insC
XM_011525334.2:c.1140+87_1140+88insC	XP_011523636.1:n.1140+87_1140+88insC
XM_011525335.3:c.1140+87_1140+88insC	XP_011523637.1:n.1140+87_1140+88insC
XM_011525336.2:c.1140+87_1140+88insC	XP_011523638.1:n.1140+87_1140+88insC
XM_011525337.2:c.1140+87_1140+88insC	XP_011523639.1:n.1140+87_1140+88insC
XM_011525338.2:c.657+87_657+88insC	XP_011523640.1:n.657+87_657+88insC
XM_011525339.3:c.1140+87_1140+88insC	XP_011523641.1:n.1140+87_1140+88insC
XM_011525340.3:c.1140+87_1140+88insC	XP_011523642.1:n.1140+87_1140+88insC
XM_011525341.3:c.1140+87_1140+88insC	XP_011523643.1:n.1140+87_1140+88insC
XM_017025200.1:c.657+87_657+88insC	XP_016880689.1:n.657+87_657+88insC
XM_017025201.1:c.597+87_597+88insC	XP_016880690.1:n.597+87_597+88insC
NM_032043.3:c.1140+87_1140+88insC MANE Select	NP_114432.2:n.1140+87_1140+88insC