Canonical Allele Identifier: CA400478643

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61776558C>T , CM000679.2:g.61776558C>T	GRCh38
NC_000017.10:g.59853919C>T , CM000679.1:g.59853919C>T	GRCh37
NC_000017.9:g.57208701C>T	NCBI36
NG_007409.2:g.92002G>A , LRG_300:g.92002G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032043.3:c.1940G>A MANE Select	NP_114432.2:p.Trp647Ter
ENST00000259008.7:c.1940G>A MANE Select	ENSP00000259008.2:p.Trp647Ter
NM_032043.2:c.1940G>A , LRG_300t1:c.1940G>A	NP_114432.2:p.Trp647Ter
ENST00000259008.6:c.1940G>A	ENSP00000259008.2:p.Trp647Ter
ENST00000577598.5:c.1940G>A	ENSP00000464654.1:p.Trp647Ter
ENST00000579028.1:c.633G>A
ENST00000579028.2:c.1522G>A	ENSP00000463827.2:n.1522G>A
ENST00000583837.5:n.22G>A
ENST00000584322.2:c.1940G>A	ENSP00000463272.2:p.Trp647Ter
ENST00000682066.1:c.1433G>A	ENSP00000507191.1:p.Trp478Ter
ENST00000682073.1:n.680G>A
ENST00000682433.1:n.1019G>A
ENST00000682453.1:c.1940G>A	ENSP00000506943.1:p.Trp647Ter
ENST00000682477.1:c.*1366G>A	ENSP00000507075.1:n.*1366G>A
ENST00000682589.1:n.7817G>A
ENST00000682611.1:c.1599G>A	ENSP00000508326.1:n.1599G>A
ENST00000682755.1:c.1718G>A	ENSP00000507660.1:p.Trp573Ter
ENST00000682989.1:c.1940G>A	ENSP00000507786.1:p.Trp647Ter
ENST00000683039.1:c.1940G>A	ENSP00000508303.1:p.Trp647Ter
ENST00000683235.1:c.1940G>A	ENSP00000507646.1:p.Trp647Ter
ENST00000683381.1:c.2000G>A	ENSP00000508184.1:p.Trp667Ter
ENST00000683535.1:n.70G>A
ENST00000684471.1:n.409-56G>A
ENST00000684584.1:c.1433G>A	ENSP00000508044.1:p.Trp478Ter
ENST00000684769.1:c.5G>A	ENSP00000507691.1:p.Trp2Ter
XM_011525332.1:c.2000G>A	XP_011523634.1:p.Trp667Ter
XM_011525332.3:c.2000G>A	XP_011523634.1:p.Trp667Ter
XM_011525333.1:c.2000G>A	XP_011523635.1:p.Trp667Ter
XM_011525333.3:c.2000G>A	XP_011523635.1:p.Trp667Ter
XM_011525334.1:c.2000G>A	XP_011523636.1:p.Trp667Ter
XM_011525334.2:c.2000G>A	XP_011523636.1:p.Trp667Ter
XM_011525335.1:c.1996-56G>A	XP_011523637.1:n.1996-56G>A
XM_011525335.3:c.1996-56G>A	XP_011523637.1:n.1996-56G>A
XM_011525336.1:c.1936-56G>A	XP_011523638.1:n.1936-56G>A
XM_011525336.2:c.1936-56G>A	XP_011523638.1:n.1936-56G>A
XM_011525337.1:c.1799G>A	XP_011523639.1:p.Trp600Ter
XM_011525337.2:c.1799G>A	XP_011523639.1:p.Trp600Ter
XM_011525338.1:c.1517G>A	XP_011523640.1:p.Trp506Ter
XM_011525338.2:c.1517G>A	XP_011523640.1:p.Trp506Ter
XM_011525339.1:c.2000G>A	XP_011523641.1:p.Trp667Ter
XM_011525339.3:c.2000G>A	XP_011523641.1:p.Trp667Ter
XM_011525340.1:c.2000G>A	XP_011523642.1:p.Trp667Ter
XM_011525340.3:c.2000G>A	XP_011523642.1:p.Trp667Ter
XM_017025200.1:c.1457G>A	XP_016880689.1:p.Trp486Ter
XM_017025201.1:c.1457G>A	XP_016880690.1:p.Trp486Ter
XM_017025202.1:c.86G>A	XP_016880691.1:p.Trp29Ter
XM_017025203.1:c.86G>A	XP_016880692.1:p.Trp29Ter