Canonical Allele Identifier: CA2269131106

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683973_61683974delinsAC , CM000679.2:g.61683973_61683974delinsAC	GRCh38
NC_000017.10:g.59761334_59761335delinsAC , CM000679.1:g.59761334_59761335delinsAC	GRCh37
NC_000017.9:g.57116116_57116117delinsAC	NCBI36
NG_007409.2:g.184586_184587delinsGT , LRG_300:g.184586_184587delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000682073.1:n.1812_1813delinsGT
ENST00000682453.1:c.3072_3073delinsGT	ENSP00000506943.1:p.Gly1024=
ENST00000682477.1:c.*2498_*2499delinsGT	ENSP00000507075.1:n.*2498_*2499delinsGT
ENST00000682589.1:n.8949_8950delinsGT
ENST00000682755.1:c.2850_2851delinsGT	ENSP00000507660.1:p.Gly950=
ENST00000682989.1:c.*163_*164delinsGT	ENSP00000507786.1:n.*163_*164delinsGT
ENST00000683039.1:c.3072_3073delinsGT	ENSP00000508303.1:p.Gly1024=
ENST00000683235.1:c.*487_*488delinsGT	ENSP00000507646.1:n.*487_*488delinsGT
ENST00000683535.1:n.1202_1203delinsGT
ENST00000684584.1:c.2235_2236delinsGT	ENSP00000508044.1:p.Gly745=
ENST00000684626.1:n.1318_1319delinsGT
ENST00000684769.1:c.1262_1263delinsGT	ENSP00000507691.1:n.1262_1263delinsGT
ENST00000259008.7:c.3072_3073delinsGT MANE Select	ENSP00000259008.2:p.Gly1024=
ENST00000259008.6:c.3072_3073delinsGT	ENSP00000259008.2:p.Gly1024=
NM_032043.2:c.3072_3073delinsGT , LRG_300t1:c.3072_3073delinsGT	NP_114432.2:p.Gly1024=
XM_011525332.1:c.3132_3133delinsGT	XP_011523634.1:p.Gly1044=
XM_011525333.1:c.3132_3133delinsGT	XP_011523635.1:p.Gly1044=
XM_011525334.1:c.3132_3133delinsGT	XP_011523636.1:p.Gly1044=
XM_011525335.1:c.3072_3073delinsGT	XP_011523637.1:p.Gly1024=
XM_011525336.1:c.3012_3013delinsGT	XP_011523638.1:p.Gly1004=
XM_011525337.1:c.2931_2932delinsGT	XP_011523639.1:p.Gly977=
XM_011525338.1:c.2649_2650delinsGT	XP_011523640.1:p.Gly883=
XM_011525332.3:c.3132_3133delinsGT	XP_011523634.1:p.Gly1044=
XM_011525333.3:c.3132_3133delinsGT	XP_011523635.1:p.Gly1044=
XM_011525334.2:c.3132_3133delinsGT	XP_011523636.1:p.Gly1044=
XM_011525335.3:c.3072_3073delinsGT	XP_011523637.1:p.Gly1024=
XM_011525336.2:c.3012_3013delinsGT	XP_011523638.1:p.Gly1004=
XM_011525337.2:c.2931_2932delinsGT	XP_011523639.1:p.Gly977=
XM_011525338.2:c.2649_2650delinsGT	XP_011523640.1:p.Gly883=
XM_017025200.1:c.2589_2590delinsGT	XP_016880689.1:p.Gly863=
XM_017025201.1:c.2589_2590delinsGT	XP_016880690.1:p.Gly863=
XM_017025202.1:c.1218_1219delinsGT	XP_016880691.1:p.Gly406=
XM_017025203.1:c.1218_1219delinsGT	XP_016880692.1:p.Gly406=
NM_032043.3:c.3072_3073delinsGT MANE Select	NP_114432.2:p.Gly1024=