Canonical Allele Identifier: CA2269144285

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61715951_61715952delinsCT , CM000679.2:g.61715951_61715952delinsCT	GRCh38
NC_000017.10:g.59793312_59793313delinsCT , CM000679.1:g.59793312_59793313delinsCT	GRCh37
NC_000017.9:g.57148094_57148095delinsCT	NCBI36
NG_007409.2:g.152608_152609delinsAG , LRG_300:g.152608_152609delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000682066.1:c.2621_2622delinsAG	ENSP00000507191.1:n.2621_2622delinsAG
ENST00000682073.1:n.1231_1232delinsAG
ENST00000682433.1:n.1570_1571delinsAG
ENST00000682453.1:c.2491_2492delinsAG	ENSP00000506943.1:p.Arg831=
ENST00000682477.1:c.*1917_*1918delinsAG	ENSP00000507075.1:n.*1917_*1918delinsAG
ENST00000682589.1:n.8368_8369delinsAG
ENST00000682755.1:c.2269_2270delinsAG	ENSP00000507660.1:p.Arg757=
ENST00000682989.1:c.2491_2492delinsAG	ENSP00000507786.1:p.Arg831=
ENST00000683039.1:c.2491_2492delinsAG	ENSP00000508303.1:p.Arg831=
ENST00000683235.1:c.2491_2492delinsAG	ENSP00000507646.1:p.Arg831=
ENST00000683535.1:n.621_622delinsAG
ENST00000684471.1:n.904_905delinsAG
ENST00000684584.1:c.1984_1985delinsAG	ENSP00000508044.1:p.Arg662=
ENST00000684626.1:n.820_821delinsAG
ENST00000684769.1:c.556_557delinsAG	ENSP00000507691.1:p.Arg186=
ENST00000259008.7:c.2491_2492delinsAG MANE Select	ENSP00000259008.2:p.Arg831=
ENST00000259008.6:c.2491_2492delinsAG	ENSP00000259008.2:p.Arg831=
ENST00000577598.5:c.2491_2492delinsAG	ENSP00000464654.1:p.Arg831=
NM_032043.2:c.2491_2492delinsAG , LRG_300t1:c.2491_2492delinsAG	NP_114432.2:p.Arg831=
XM_011525332.1:c.2551_2552delinsAG	XP_011523634.1:p.Arg851=
XM_011525333.1:c.2551_2552delinsAG	XP_011523635.1:p.Arg851=
XM_011525334.1:c.2551_2552delinsAG	XP_011523636.1:p.Arg851=
XM_011525335.1:c.2491_2492delinsAG	XP_011523637.1:p.Arg831=
XM_011525336.1:c.2431_2432delinsAG	XP_011523638.1:p.Arg811=
XM_011525337.1:c.2350_2351delinsAG	XP_011523639.1:p.Arg784=
XM_011525338.1:c.2068_2069delinsAG	XP_011523640.1:p.Arg690=
XM_011525340.1:c.2551_2552delinsAG	XP_011523642.1:p.Arg851=
XM_011525332.3:c.2551_2552delinsAG	XP_011523634.1:p.Arg851=
XM_011525333.3:c.2551_2552delinsAG	XP_011523635.1:p.Arg851=
XM_011525334.2:c.2551_2552delinsAG	XP_011523636.1:p.Arg851=
XM_011525335.3:c.2491_2492delinsAG	XP_011523637.1:p.Arg831=
XM_011525336.2:c.2431_2432delinsAG	XP_011523638.1:p.Arg811=
XM_011525337.2:c.2350_2351delinsAG	XP_011523639.1:p.Arg784=
XM_011525338.2:c.2068_2069delinsAG	XP_011523640.1:p.Arg690=
XM_011525340.3:c.2551_2552delinsAG	XP_011523642.1:p.Arg851=
XM_017025200.1:c.2008_2009delinsAG	XP_016880689.1:p.Arg670=
XM_017025201.1:c.2008_2009delinsAG	XP_016880690.1:p.Arg670=
XM_017025202.1:c.637_638delinsAG	XP_016880691.1:p.Arg213=
XM_017025203.1:c.637_638delinsAG	XP_016880692.1:p.Arg213=
NM_032043.3:c.2491_2492delinsAG MANE Select	NP_114432.2:p.Arg831=