Canonical Allele Identifier: CA2269178604

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61799090_61799093delinsATCT , CM000679.2:g.61799090_61799093delinsATCT	GRCh38
NC_000017.10:g.59876451_59876454delinsATCT , CM000679.1:g.59876451_59876454delinsATCT	GRCh37
NC_000017.9:g.57231233_57231236delinsATCT	NCBI36
NG_007409.2:g.69467_69470delinsAGAT , LRG_300:g.69467_69470delinsAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.833+7_833+10delinsAGAT	ENSP00000463827.2:n.833+7_833+10delinsAGAT
ENST00000584322.2:c.1340+7_1340+10delinsAGAT	ENSP00000463272.2:n.1340+7_1340+10delinsAGAT
ENST00000682066.1:c.833+7_833+10delinsAGAT	ENSP00000507191.1:n.833+7_833+10delinsAGAT
ENST00000682453.1:c.1340+7_1340+10delinsAGAT	ENSP00000506943.1:n.1340+7_1340+10delinsAGAT
ENST00000682477.1:c.1340+7_1340+10delinsAGAT	ENSP00000507075.1:n.1340+7_1340+10delinsAGAT
ENST00000682589.1:n.3081+7_3081+10delinsAGAT
ENST00000682611.1:c.833+7_833+10delinsAGAT	ENSP00000508326.1:n.833+7_833+10delinsAGAT
ENST00000682755.1:c.1118+7_1118+10delinsAGAT	ENSP00000507660.1:n.1118+7_1118+10delinsAGAT
ENST00000682989.1:c.1340+7_1340+10delinsAGAT	ENSP00000507786.1:n.1340+7_1340+10delinsAGAT
ENST00000683039.1:c.1340+7_1340+10delinsAGAT	ENSP00000508303.1:n.1340+7_1340+10delinsAGAT
ENST00000683235.1:c.1340+7_1340+10delinsAGAT	ENSP00000507646.1:n.1340+7_1340+10delinsAGAT
ENST00000683381.1:c.1340+7_1340+10delinsAGAT	ENSP00000508184.1:n.1340+7_1340+10delinsAGAT
ENST00000684584.1:c.833+7_833+10delinsAGAT	ENSP00000508044.1:n.833+7_833+10delinsAGAT
ENST00000259008.7:c.1340+7_1340+10delinsAGAT MANE Select	ENSP00000259008.2:n.1340+7_1340+10delinsAGAT
ENST00000259008.6:c.1340+7_1340+10delinsAGAT	ENSP00000259008.2:n.1340+7_1340+10delinsAGAT
ENST00000577598.5:c.1340+7_1340+10delinsAGAT	ENSP00000464654.1:n.1340+7_1340+10delinsAGAT
NM_032043.2:c.1340+7_1340+10delinsAGAT , LRG_300t1:c.1340+7_1340+10delinsAGAT	NP_114432.2:n.1340+7_1340+10delinsAGAT
XM_011525332.1:c.1340+7_1340+10delinsAGAT	XP_011523634.1:n.1340+7_1340+10delinsAGAT
XM_011525333.1:c.1340+7_1340+10delinsAGAT	XP_011523635.1:n.1340+7_1340+10delinsAGAT
XM_011525334.1:c.1340+7_1340+10delinsAGAT	XP_011523636.1:n.1340+7_1340+10delinsAGAT
XM_011525335.1:c.1340+7_1340+10delinsAGAT	XP_011523637.1:n.1340+7_1340+10delinsAGAT
XM_011525336.1:c.1340+7_1340+10delinsAGAT	XP_011523638.1:n.1340+7_1340+10delinsAGAT
XM_011525337.1:c.1340+7_1340+10delinsAGAT	XP_011523639.1:n.1340+7_1340+10delinsAGAT
XM_011525338.1:c.857+7_857+10delinsAGAT	XP_011523640.1:n.857+7_857+10delinsAGAT
XM_011525339.1:c.1340+7_1340+10delinsAGAT	XP_011523641.1:n.1340+7_1340+10delinsAGAT
XM_011525340.1:c.1340+7_1340+10delinsAGAT	XP_011523642.1:n.1340+7_1340+10delinsAGAT
XM_011525341.1:c.1340+7_1340+10delinsAGAT	XP_011523643.1:n.1340+7_1340+10delinsAGAT
XM_011525332.3:c.1340+7_1340+10delinsAGAT	XP_011523634.1:n.1340+7_1340+10delinsAGAT
XM_011525333.3:c.1340+7_1340+10delinsAGAT	XP_011523635.1:n.1340+7_1340+10delinsAGAT
XM_011525334.2:c.1340+7_1340+10delinsAGAT	XP_011523636.1:n.1340+7_1340+10delinsAGAT
XM_011525335.3:c.1340+7_1340+10delinsAGAT	XP_011523637.1:n.1340+7_1340+10delinsAGAT
XM_011525336.2:c.1340+7_1340+10delinsAGAT	XP_011523638.1:n.1340+7_1340+10delinsAGAT
XM_011525337.2:c.1340+7_1340+10delinsAGAT	XP_011523639.1:n.1340+7_1340+10delinsAGAT
XM_011525338.2:c.857+7_857+10delinsAGAT	XP_011523640.1:n.857+7_857+10delinsAGAT
XM_011525339.3:c.1340+7_1340+10delinsAGAT	XP_011523641.1:n.1340+7_1340+10delinsAGAT
XM_011525340.3:c.1340+7_1340+10delinsAGAT	XP_011523642.1:n.1340+7_1340+10delinsAGAT
XM_011525341.3:c.1340+7_1340+10delinsAGAT	XP_011523643.1:n.1340+7_1340+10delinsAGAT
XM_017025200.1:c.857+7_857+10delinsAGAT	XP_016880689.1:n.857+7_857+10delinsAGAT
XM_017025201.1:c.797+7_797+10delinsAGAT	XP_016880690.1:n.797+7_797+10delinsAGAT
NM_032043.3:c.1340+7_1340+10delinsAGAT MANE Select	NP_114432.2:n.1340+7_1340+10delinsAGAT