Canonical Allele Identifier: CA2269130903

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683644_61683645delinsAG , CM000679.2:g.61683644_61683645delinsAG	GRCh38
NC_000017.10:g.59761005_59761006delinsAG , CM000679.1:g.59761005_59761006delinsAG	GRCh37
NC_000017.9:g.57115787_57115788delinsAG	NCBI36
NG_007409.2:g.184915_184916delinsCT , LRG_300:g.184915_184916delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2141_2142delinsCT
ENST00000682453.1:c.3401_3402delinsCT	ENSP00000506943.1:p.Pro1134=
ENST00000682477.1:c.*2827_*2828delinsCT	ENSP00000507075.1:n.*2827_*2828delinsCT
ENST00000682589.1:n.9278_9279delinsCT
ENST00000682755.1:c.3179_3180delinsCT	ENSP00000507660.1:p.Pro1060=
ENST00000682989.1:c.*492_*493delinsCT	ENSP00000507786.1:n.*492_*493delinsCT
ENST00000683039.1:c.3401_3402delinsCT	ENSP00000508303.1:p.Pro1134=
ENST00000683235.1:c.*816_*817delinsCT	ENSP00000507646.1:n.*816_*817delinsCT
ENST00000683535.1:n.1531_1532delinsCT
ENST00000684584.1:c.2564_2565delinsCT	ENSP00000508044.1:p.Pro855=
ENST00000684626.1:n.1647_1648delinsCT
ENST00000684769.1:c.1591_1592delinsCT	ENSP00000507691.1:n.1591_1592delinsCT
ENST00000259008.7:c.3401_3402delinsCT MANE Select	ENSP00000259008.2:p.Pro1134=
ENST00000259008.6:c.3401_3402delinsCT	ENSP00000259008.2:p.Pro1134=
NM_032043.2:c.3401_3402delinsCT , LRG_300t1:c.3401_3402delinsCT	NP_114432.2:p.Pro1134=
XM_011525332.1:c.3461_3462delinsCT	XP_011523634.1:p.Pro1154=
XM_011525333.1:c.3461_3462delinsCT	XP_011523635.1:p.Pro1154=
XM_011525334.1:c.3461_3462delinsCT	XP_011523636.1:p.Pro1154=
XM_011525335.1:c.3401_3402delinsCT	XP_011523637.1:p.Pro1134=
XM_011525336.1:c.3341_3342delinsCT	XP_011523638.1:p.Pro1114=
XM_011525337.1:c.3260_3261delinsCT	XP_011523639.1:p.Pro1087=
XM_011525338.1:c.2978_2979delinsCT	XP_011523640.1:p.Pro993=
XM_011525332.3:c.3461_3462delinsCT	XP_011523634.1:p.Pro1154=
XM_011525333.3:c.3461_3462delinsCT	XP_011523635.1:p.Pro1154=
XM_011525334.2:c.3461_3462delinsCT	XP_011523636.1:p.Pro1154=
XM_011525335.3:c.3401_3402delinsCT	XP_011523637.1:p.Pro1134=
XM_011525336.2:c.3341_3342delinsCT	XP_011523638.1:p.Pro1114=
XM_011525337.2:c.3260_3261delinsCT	XP_011523639.1:p.Pro1087=
XM_011525338.2:c.2978_2979delinsCT	XP_011523640.1:p.Pro993=
XM_017025200.1:c.2918_2919delinsCT	XP_016880689.1:p.Pro973=
XM_017025201.1:c.2918_2919delinsCT	XP_016880690.1:p.Pro973=
XM_017025202.1:c.1547_1548delinsCT	XP_016880691.1:p.Pro516=
XM_017025203.1:c.1547_1548delinsCT	XP_016880692.1:p.Pro516=
NM_032043.3:c.3401_3402delinsCT MANE Select	NP_114432.2:p.Pro1134=