Canonical Allele Identifier: CA2639156703

Gene: BRIP1

Linked Data

• gnomAD v4: 17-61801161-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61801161_61801162insT , CM000679.2:g.61801161_61801162insT	GRCh38
NC_000017.10:g.59878522_59878523insT , CM000679.1:g.59878522_59878523insT	GRCh37
NC_000017.9:g.57233304_57233305insT	NCBI36
NG_007409.2:g.67398_67399insA , LRG_300:g.67398_67399insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.633+91_633+92insA	ENSP00000463827.2:n.633+91_633+92insA
ENST00000584322.2:c.1140+91_1140+92insA	ENSP00000463272.2:n.1140+91_1140+92insA
ENST00000682066.1:c.633+91_633+92insA	ENSP00000507191.1:n.633+91_633+92insA
ENST00000682453.1:c.1140+91_1140+92insA	ENSP00000506943.1:n.1140+91_1140+92insA
ENST00000682477.1:c.1140+91_1140+92insA	ENSP00000507075.1:n.1140+91_1140+92insA
ENST00000682589.1:n.2881+91_2881+92insA
ENST00000682611.1:c.633+91_633+92insA	ENSP00000508326.1:n.633+91_633+92insA
ENST00000682755.1:c.919-1863_919-1862insA	ENSP00000507660.1:n.919-1863_919-1862insA
ENST00000682989.1:c.1140+91_1140+92insA	ENSP00000507786.1:n.1140+91_1140+92insA
ENST00000683039.1:c.1140+91_1140+92insA	ENSP00000508303.1:n.1140+91_1140+92insA
ENST00000683235.1:c.1140+91_1140+92insA	ENSP00000507646.1:n.1140+91_1140+92insA
ENST00000683381.1:c.1140+91_1140+92insA	ENSP00000508184.1:n.1140+91_1140+92insA
ENST00000683692.1:c.718+91_718+92insA	ENSP00000507964.1:n.718+91_718+92insA
ENST00000684584.1:c.633+91_633+92insA	ENSP00000508044.1:n.633+91_633+92insA
ENST00000259008.7:c.1140+91_1140+92insA MANE Select	ENSP00000259008.2:n.1140+91_1140+92insA
ENST00000259008.6:c.1140+91_1140+92insA	ENSP00000259008.2:n.1140+91_1140+92insA
ENST00000577598.5:c.1140+91_1140+92insA	ENSP00000464654.1:n.1140+91_1140+92insA
NM_032043.2:c.1140+91_1140+92insA , LRG_300t1:c.1140+91_1140+92insA	NP_114432.2:n.1140+91_1140+92insA
XM_011525332.1:c.1140+91_1140+92insA	XP_011523634.1:n.1140+91_1140+92insA
XM_011525333.1:c.1140+91_1140+92insA	XP_011523635.1:n.1140+91_1140+92insA
XM_011525334.1:c.1140+91_1140+92insA	XP_011523636.1:n.1140+91_1140+92insA
XM_011525335.1:c.1140+91_1140+92insA	XP_011523637.1:n.1140+91_1140+92insA
XM_011525336.1:c.1140+91_1140+92insA	XP_011523638.1:n.1140+91_1140+92insA
XM_011525337.1:c.1140+91_1140+92insA	XP_011523639.1:n.1140+91_1140+92insA
XM_011525338.1:c.657+91_657+92insA	XP_011523640.1:n.657+91_657+92insA
XM_011525339.1:c.1140+91_1140+92insA	XP_011523641.1:n.1140+91_1140+92insA
XM_011525340.1:c.1140+91_1140+92insA	XP_011523642.1:n.1140+91_1140+92insA
XM_011525341.1:c.1140+91_1140+92insA	XP_011523643.1:n.1140+91_1140+92insA
XM_011525332.3:c.1140+91_1140+92insA	XP_011523634.1:n.1140+91_1140+92insA
XM_011525333.3:c.1140+91_1140+92insA	XP_011523635.1:n.1140+91_1140+92insA
XM_011525334.2:c.1140+91_1140+92insA	XP_011523636.1:n.1140+91_1140+92insA
XM_011525335.3:c.1140+91_1140+92insA	XP_011523637.1:n.1140+91_1140+92insA
XM_011525336.2:c.1140+91_1140+92insA	XP_011523638.1:n.1140+91_1140+92insA
XM_011525337.2:c.1140+91_1140+92insA	XP_011523639.1:n.1140+91_1140+92insA
XM_011525338.2:c.657+91_657+92insA	XP_011523640.1:n.657+91_657+92insA
XM_011525339.3:c.1140+91_1140+92insA	XP_011523641.1:n.1140+91_1140+92insA
XM_011525340.3:c.1140+91_1140+92insA	XP_011523642.1:n.1140+91_1140+92insA
XM_011525341.3:c.1140+91_1140+92insA	XP_011523643.1:n.1140+91_1140+92insA
XM_017025200.1:c.657+91_657+92insA	XP_016880689.1:n.657+91_657+92insA
XM_017025201.1:c.597+91_597+92insA	XP_016880690.1:n.597+91_597+92insA
NM_032043.3:c.1140+91_1140+92insA MANE Select	NP_114432.2:n.1140+91_1140+92insA