Canonical Allele Identifier: CA985262222

Gene: BRIP1

Linked Data

• gnomAD v3: 17-61780237-C-CA
• gnomAD v4: 17-61780237-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61780237_61780238insA , CM000679.2:g.61780237_61780238insA	GRCh38
NC_000017.10:g.59857598_59857599insA , CM000679.1:g.59857598_59857599insA	GRCh37
NC_000017.9:g.57212380_57212381insA	NCBI36
NG_007409.2:g.88322_88323insT , LRG_300:g.88322_88323insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.1517+23_1517+24insT	ENSP00000463827.2:n.1517+23_1517+24insT
ENST00000584322.2:c.1935+23_1935+24insT	ENSP00000463272.2:n.1935+23_1935+24insT
ENST00000682066.1:c.1428+23_1428+24insT	ENSP00000507191.1:n.1428+23_1428+24insT
ENST00000682073.1:n.675+23_675+24insT
ENST00000682453.1:c.1935+23_1935+24insT	ENSP00000506943.1:n.1935+23_1935+24insT
ENST00000682477.1:c.*1361+23_*1361+24insT	ENSP00000507075.1:n.*1361+23_*1361+24insT
ENST00000682589.1:n.4137_4138insT
ENST00000682611.1:c.1428+23_1428+24insT	ENSP00000508326.1:n.1428+23_1428+24insT
ENST00000682755.1:c.1713+23_1713+24insT	ENSP00000507660.1:n.1713+23_1713+24insT
ENST00000682989.1:c.1935+23_1935+24insT	ENSP00000507786.1:n.1935+23_1935+24insT
ENST00000683039.1:c.1935+23_1935+24insT	ENSP00000508303.1:n.1935+23_1935+24insT
ENST00000683235.1:c.1935+23_1935+24insT	ENSP00000507646.1:n.1935+23_1935+24insT
ENST00000683381.1:c.1935+23_1935+24insT	ENSP00000508184.1:n.1935+23_1935+24insT
ENST00000684471.1:n.408+23_408+24insT
ENST00000684584.1:c.1428+23_1428+24insT	ENSP00000508044.1:n.1428+23_1428+24insT
ENST00000259008.7:c.1935+23_1935+24insT MANE Select	ENSP00000259008.2:n.1935+23_1935+24insT
ENST00000259008.6:c.1935+23_1935+24insT	ENSP00000259008.2:n.1935+23_1935+24insT
ENST00000577598.5:c.1935+23_1935+24insT	ENSP00000464654.1:n.1935+23_1935+24insT
ENST00000579028.1:c.628+23_628+24insT
ENST00000583837.5:n.17+23_17+24insT
NM_032043.2:c.1935+23_1935+24insT , LRG_300t1:c.1935+23_1935+24insT	NP_114432.2:n.1935+23_1935+24insT
XM_011525332.1:c.1935+23_1935+24insT	XP_011523634.1:n.1935+23_1935+24insT
XM_011525333.1:c.1935+23_1935+24insT	XP_011523635.1:n.1935+23_1935+24insT
XM_011525334.1:c.1935+23_1935+24insT	XP_011523636.1:n.1935+23_1935+24insT
XM_011525335.1:c.1935+23_1935+24insT	XP_011523637.1:n.1935+23_1935+24insT
XM_011525336.1:c.1935+23_1935+24insT	XP_011523638.1:n.1935+23_1935+24insT
XM_011525337.1:c.1794+602_1794+603insT	XP_011523639.1:n.1794+602_1794+603insT
XM_011525338.1:c.1452+23_1452+24insT	XP_011523640.1:n.1452+23_1452+24insT
XM_011525339.1:c.1935+23_1935+24insT	XP_011523641.1:n.1935+23_1935+24insT
XM_011525340.1:c.1935+23_1935+24insT	XP_011523642.1:n.1935+23_1935+24insT
XM_011525341.1:c.1935+23_1935+24insT	XP_011523643.1:n.1935+23_1935+24insT
XM_011525332.3:c.1935+23_1935+24insT	XP_011523634.1:n.1935+23_1935+24insT
XM_011525333.3:c.1935+23_1935+24insT	XP_011523635.1:n.1935+23_1935+24insT
XM_011525334.2:c.1935+23_1935+24insT	XP_011523636.1:n.1935+23_1935+24insT
XM_011525335.3:c.1935+23_1935+24insT	XP_011523637.1:n.1935+23_1935+24insT
XM_011525336.2:c.1935+23_1935+24insT	XP_011523638.1:n.1935+23_1935+24insT
XM_011525337.2:c.1794+602_1794+603insT	XP_011523639.1:n.1794+602_1794+603insT
XM_011525338.2:c.1452+23_1452+24insT	XP_011523640.1:n.1452+23_1452+24insT
XM_011525339.3:c.1935+23_1935+24insT	XP_011523641.1:n.1935+23_1935+24insT
XM_011525340.3:c.1935+23_1935+24insT	XP_011523642.1:n.1935+23_1935+24insT
XM_011525341.3:c.1935+23_1935+24insT	XP_011523643.1:n.1935+23_1935+24insT
XM_017025200.1:c.1452+23_1452+24insT	XP_016880689.1:n.1452+23_1452+24insT
XM_017025201.1:c.1392+23_1392+24insT	XP_016880690.1:n.1392+23_1392+24insT
XM_017025203.1:c.-26+23_-26+24insT	XP_016880692.1:n.-26+23_-26+24insT
NM_032043.3:c.1935+23_1935+24insT MANE Select	NP_114432.2:n.1935+23_1935+24insT