Canonical Allele Identifier: CA891843743

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 570962
• ClinVar RCV Id: RCV000691968 ; RCV001190188 ; RCV002282331 ; RCV003492131
• dbSNP Id: rs1555572620

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683634_61683635delinsAG , CM000679.2:g.61683634_61683635delinsAG	GRCh38
NC_000017.10:g.59760995_59760996delinsAG , CM000679.1:g.59760995_59760996delinsAG	GRCh37
NC_000017.9:g.57115777_57115778delinsAG	NCBI36
NG_007409.2:g.184925_184926delinsCT , LRG_300:g.184925_184926delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2151_2152delinsCT
ENST00000682453.1:c.3411_3412delinsCT	ENSP00000506943.1:p.Asp1138Tyr
ENST00000682477.1:c.*2837_*2838delinsCT	ENSP00000507075.1:n.*2837_*2838delinsCT
ENST00000682589.1:n.9288_9289delinsCT
ENST00000682755.1:c.3189_3190delinsCT	ENSP00000507660.1:p.Asp1064Tyr
ENST00000682989.1:c.*502_*503delinsCT	ENSP00000507786.1:n.*502_*503delinsCT
ENST00000683039.1:c.3411_3412delinsCT	ENSP00000508303.1:p.Asp1138Tyr
ENST00000683235.1:c.*826_*827delinsCT	ENSP00000507646.1:n.*826_*827delinsCT
ENST00000683535.1:n.1541_1542delinsCT
ENST00000684584.1:c.2574_2575delinsCT	ENSP00000508044.1:p.Asp859Tyr
ENST00000684626.1:n.1657_1658delinsCT
ENST00000684769.1:c.1601_1602delinsCT	ENSP00000507691.1:n.1601_1602delinsCT
ENST00000259008.7:c.3411_3412delinsCT MANE Select	ENSP00000259008.2:p.Asp1138Tyr
ENST00000259008.6:c.3411_3412delinsCT	ENSP00000259008.2:p.Asp1138Tyr
NM_032043.2:c.3411_3412delinsCT , LRG_300t1:c.3411_3412delinsCT	NP_114432.2:p.Asp1138Tyr
XM_011525332.1:c.3471_3472delinsCT	XP_011523634.1:p.Asp1158Tyr
XM_011525333.1:c.3471_3472delinsCT	XP_011523635.1:p.Asp1158Tyr
XM_011525334.1:c.3471_3472delinsCT	XP_011523636.1:p.Asp1158Tyr
XM_011525335.1:c.3411_3412delinsCT	XP_011523637.1:p.Asp1138Tyr
XM_011525336.1:c.3351_3352delinsCT	XP_011523638.1:p.Asp1118Tyr
XM_011525337.1:c.3270_3271delinsCT	XP_011523639.1:p.Asp1091Tyr
XM_011525338.1:c.2988_2989delinsCT	XP_011523640.1:p.Asp997Tyr
XM_011525332.3:c.3471_3472delinsCT	XP_011523634.1:p.Asp1158Tyr
XM_011525333.3:c.3471_3472delinsCT	XP_011523635.1:p.Asp1158Tyr
XM_011525334.2:c.3471_3472delinsCT	XP_011523636.1:p.Asp1158Tyr
XM_011525335.3:c.3411_3412delinsCT	XP_011523637.1:p.Asp1138Tyr
XM_011525336.2:c.3351_3352delinsCT	XP_011523638.1:p.Asp1118Tyr
XM_011525337.2:c.3270_3271delinsCT	XP_011523639.1:p.Asp1091Tyr
XM_011525338.2:c.2988_2989delinsCT	XP_011523640.1:p.Asp997Tyr
XM_017025200.1:c.2928_2929delinsCT	XP_016880689.1:p.Asp977Tyr
XM_017025201.1:c.2928_2929delinsCT	XP_016880690.1:p.Asp977Tyr
XM_017025202.1:c.1557_1558delinsCT	XP_016880691.1:p.Asp520Tyr
XM_017025203.1:c.1557_1558delinsCT	XP_016880692.1:p.Asp520Tyr
NM_032043.3:c.3411_3412delinsCT MANE Select	NP_114432.2:p.Asp1138Tyr