Canonical Allele Identifier: CA2269131136

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61684020C= , CM000679.2:g.61684020C=	GRCh38
NC_000017.10:g.59761381C= , CM000679.1:g.59761381C=	GRCh37
NC_000017.9:g.57116163C=	NCBI36
NG_007409.2:g.184540G= , LRG_300:g.184540G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1766G=
ENST00000682453.1:c.3026G=	ENSP00000506943.1:p.Gly1009=
ENST00000682477.1:c.*2452G=	ENSP00000507075.1:n.*2452G=
ENST00000682589.1:n.8903G=
ENST00000682755.1:c.2804G=	ENSP00000507660.1:p.Gly935=
ENST00000682989.1:c.*117G=	ENSP00000507786.1:n.*117G=
ENST00000683039.1:c.3026G=	ENSP00000508303.1:p.Gly1009=
ENST00000683235.1:c.*441G=	ENSP00000507646.1:n.*441G=
ENST00000683535.1:n.1156G=
ENST00000684584.1:c.2189G=	ENSP00000508044.1:p.Gly730=
ENST00000684626.1:n.1272G=
ENST00000684769.1:c.1216G=	ENSP00000507691.1:n.1216G=
ENST00000259008.7:c.3026G= MANE Select	ENSP00000259008.2:p.Gly1009=
ENST00000259008.6:c.3026G=	ENSP00000259008.2:p.Gly1009=
NM_032043.2:c.3026G= , LRG_300t1:c.3026G=	NP_114432.2:p.Gly1009=
XM_011525332.1:c.3086G=	XP_011523634.1:p.Gly1029=
XM_011525333.1:c.3086G=	XP_011523635.1:p.Gly1029=
XM_011525334.1:c.3086G=	XP_011523636.1:p.Gly1029=
XM_011525335.1:c.3026G=	XP_011523637.1:p.Gly1009=
XM_011525336.1:c.2966G=	XP_011523638.1:p.Gly989=
XM_011525337.1:c.2885G=	XP_011523639.1:p.Gly962=
XM_011525338.1:c.2603G=	XP_011523640.1:p.Gly868=
XM_011525332.3:c.3086G=	XP_011523634.1:p.Gly1029=
XM_011525333.3:c.3086G=	XP_011523635.1:p.Gly1029=
XM_011525334.2:c.3086G=	XP_011523636.1:p.Gly1029=
XM_011525335.3:c.3026G=	XP_011523637.1:p.Gly1009=
XM_011525336.2:c.2966G=	XP_011523638.1:p.Gly989=
XM_011525337.2:c.2885G=	XP_011523639.1:p.Gly962=
XM_011525338.2:c.2603G=	XP_011523640.1:p.Gly868=
XM_017025200.1:c.2543G=	XP_016880689.1:p.Gly848=
XM_017025201.1:c.2543G=	XP_016880690.1:p.Gly848=
XM_017025202.1:c.1172G=	XP_016880691.1:p.Gly391=
XM_017025203.1:c.1172G=	XP_016880692.1:p.Gly391=
NM_032043.3:c.3026G= MANE Select	NP_114432.2:p.Gly1009=