Canonical Allele Identifier: CA2269161062

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61758386_61758387delinsGC , CM000679.2:g.61758386_61758387delinsGC	GRCh38
NC_000017.10:g.59835747_59835748delinsGC , CM000679.1:g.59835747_59835748delinsGC	GRCh37
NC_000017.9:g.57190529_57190530delinsGC	NCBI36
NG_007409.2:g.110173_110174delinsGC , LRG_300:g.110173_110174delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.1680-13796_1680-13795delinsGC	ENSP00000463827.2:n.1680-13796_1680-13795delinsGC
ENST00000584322.2:c.2098-13796_2098-13795delinsGC	ENSP00000463272.2:n.2098-13796_2098-13795delinsGC
ENST00000682066.1:c.2227+287_2227+288delinsGC	ENSP00000507191.1:n.2227+287_2227+288delinsGC
ENST00000682073.1:n.838-13796_838-13795delinsGC
ENST00000682433.1:n.1177-13796_1177-13795delinsGC
ENST00000682453.1:c.2098-13796_2098-13795delinsGC	ENSP00000506943.1:n.2098-13796_2098-13795delinsGC
ENST00000682477.1:c.*1524-13796_*1524-13795delinsGC	ENSP00000507075.1:n.*1524-13796_*1524-13795delinsGC
ENST00000682589.1:n.7975-13796_7975-13795delinsGC
ENST00000682755.1:c.1876-13796_1876-13795delinsGC	ENSP00000507660.1:n.1876-13796_1876-13795delinsGC
ENST00000682989.1:c.2098-13796_2098-13795delinsGC	ENSP00000507786.1:n.2098-13796_2098-13795delinsGC
ENST00000683039.1:c.2098-13796_2098-13795delinsGC	ENSP00000508303.1:n.2098-13796_2098-13795delinsGC
ENST00000683235.1:c.2098-13796_2098-13795delinsGC	ENSP00000507646.1:n.2098-13796_2098-13795delinsGC
ENST00000683381.1:c.2158-13796_2158-13795delinsGC	ENSP00000508184.1:n.2158-13796_2158-13795delinsGC
ENST00000683535.1:n.228-13796_228-13795delinsGC
ENST00000684471.1:n.511-13796_511-13795delinsGC
ENST00000684584.1:c.1591-13796_1591-13795delinsGC	ENSP00000508044.1:n.1591-13796_1591-13795delinsGC
ENST00000684769.1:c.163-13796_163-13795delinsGC	ENSP00000507691.1:n.163-13796_163-13795delinsGC
ENST00000259008.7:c.2098-13796_2098-13795delinsGC MANE Select	ENSP00000259008.2:n.2098-13796_2098-13795delinsGC
ENST00000259008.6:c.2098-13796_2098-13795delinsGC	ENSP00000259008.2:n.2098-13796_2098-13795delinsGC
ENST00000577598.5:c.2098-13796_2098-13795delinsGC	ENSP00000464654.1:n.2098-13796_2098-13795delinsGC
ENST00000584322.1:c.81-13796_81-13795delinsGC
NM_032043.2:c.2098-13796_2098-13795delinsGC , LRG_300t1:c.2098-13796_2098-13795delinsGC	NP_114432.2:n.2098-13796_2098-13795delinsGC
XM_011525332.1:c.2158-13796_2158-13795delinsGC	XP_011523634.1:n.2158-13796_2158-13795delinsGC
XM_011525333.1:c.2158-13796_2158-13795delinsGC	XP_011523635.1:n.2158-13796_2158-13795delinsGC
XM_011525334.1:c.2158-13796_2158-13795delinsGC	XP_011523636.1:n.2158-13796_2158-13795delinsGC
XM_011525335.1:c.2098-13796_2098-13795delinsGC	XP_011523637.1:n.2098-13796_2098-13795delinsGC
XM_011525336.1:c.2038-13796_2038-13795delinsGC	XP_011523638.1:n.2038-13796_2038-13795delinsGC
XM_011525337.1:c.1957-13796_1957-13795delinsGC	XP_011523639.1:n.1957-13796_1957-13795delinsGC
XM_011525338.1:c.1675-13796_1675-13795delinsGC	XP_011523640.1:n.1675-13796_1675-13795delinsGC
XM_011525339.1:c.2158-13796_2158-13795delinsGC	XP_011523641.1:n.2158-13796_2158-13795delinsGC
XM_011525340.1:c.2158-13796_2158-13795delinsGC	XP_011523642.1:n.2158-13796_2158-13795delinsGC
XM_011525332.3:c.2158-13796_2158-13795delinsGC	XP_011523634.1:n.2158-13796_2158-13795delinsGC
XM_011525333.3:c.2158-13796_2158-13795delinsGC	XP_011523635.1:n.2158-13796_2158-13795delinsGC
XM_011525334.2:c.2158-13796_2158-13795delinsGC	XP_011523636.1:n.2158-13796_2158-13795delinsGC
XM_011525335.3:c.2098-13796_2098-13795delinsGC	XP_011523637.1:n.2098-13796_2098-13795delinsGC
XM_011525336.2:c.2038-13796_2038-13795delinsGC	XP_011523638.1:n.2038-13796_2038-13795delinsGC
XM_011525337.2:c.1957-13796_1957-13795delinsGC	XP_011523639.1:n.1957-13796_1957-13795delinsGC
XM_011525338.2:c.1675-13796_1675-13795delinsGC	XP_011523640.1:n.1675-13796_1675-13795delinsGC
XM_011525339.3:c.2158-13796_2158-13795delinsGC	XP_011523641.1:n.2158-13796_2158-13795delinsGC
XM_011525340.3:c.2158-13796_2158-13795delinsGC	XP_011523642.1:n.2158-13796_2158-13795delinsGC
XM_017025200.1:c.1615-13796_1615-13795delinsGC	XP_016880689.1:n.1615-13796_1615-13795delinsGC
XM_017025201.1:c.1615-13796_1615-13795delinsGC	XP_016880690.1:n.1615-13796_1615-13795delinsGC
XM_017025202.1:c.244-13796_244-13795delinsGC	XP_016880691.1:n.244-13796_244-13795delinsGC
XM_017025203.1:c.244-13796_244-13795delinsGC	XP_016880692.1:n.244-13796_244-13795delinsGC
NM_032043.3:c.2098-13796_2098-13795delinsGC MANE Select	NP_114432.2:n.2098-13796_2098-13795delinsGC