Canonical Allele Identifier: CA2269130981

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683770C= , CM000679.2:g.61683770C=	GRCh38
NC_000017.10:g.59761131C= , CM000679.1:g.59761131C=	GRCh37
NC_000017.9:g.57115913C=	NCBI36
NG_007409.2:g.184790G= , LRG_300:g.184790G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2016G=
ENST00000682453.1:c.3276G=	ENSP00000506943.1:p.Pro1092=
ENST00000682477.1:c.*2702G=	ENSP00000507075.1:n.*2702G=
ENST00000682589.1:n.9153G=
ENST00000682755.1:c.3054G=	ENSP00000507660.1:p.Pro1018=
ENST00000682989.1:c.*367G=	ENSP00000507786.1:n.*367G=
ENST00000683039.1:c.3276G=	ENSP00000508303.1:p.Pro1092=
ENST00000683235.1:c.*691G=	ENSP00000507646.1:n.*691G=
ENST00000683535.1:n.1406G=
ENST00000684584.1:c.2439G=	ENSP00000508044.1:p.Pro813=
ENST00000684626.1:n.1522G=
ENST00000684769.1:c.1466G=	ENSP00000507691.1:n.1466G=
ENST00000259008.7:c.3276G= MANE Select	ENSP00000259008.2:p.Pro1092=
ENST00000259008.6:c.3276G=	ENSP00000259008.2:p.Pro1092=
NM_032043.2:c.3276G= , LRG_300t1:c.3276G=	NP_114432.2:p.Pro1092=
XM_011525332.1:c.3336G=	XP_011523634.1:p.Pro1112=
XM_011525333.1:c.3336G=	XP_011523635.1:p.Pro1112=
XM_011525334.1:c.3336G=	XP_011523636.1:p.Pro1112=
XM_011525335.1:c.3276G=	XP_011523637.1:p.Pro1092=
XM_011525336.1:c.3216G=	XP_011523638.1:p.Pro1072=
XM_011525337.1:c.3135G=	XP_011523639.1:p.Pro1045=
XM_011525338.1:c.2853G=	XP_011523640.1:p.Pro951=
XM_011525332.3:c.3336G=	XP_011523634.1:p.Pro1112=
XM_011525333.3:c.3336G=	XP_011523635.1:p.Pro1112=
XM_011525334.2:c.3336G=	XP_011523636.1:p.Pro1112=
XM_011525335.3:c.3276G=	XP_011523637.1:p.Pro1092=
XM_011525336.2:c.3216G=	XP_011523638.1:p.Pro1072=
XM_011525337.2:c.3135G=	XP_011523639.1:p.Pro1045=
XM_011525338.2:c.2853G=	XP_011523640.1:p.Pro951=
XM_017025200.1:c.2793G=	XP_016880689.1:p.Pro931=
XM_017025201.1:c.2793G=	XP_016880690.1:p.Pro931=
XM_017025202.1:c.1422G=	XP_016880691.1:p.Pro474=
XM_017025203.1:c.1422G=	XP_016880692.1:p.Pro474=
NM_032043.3:c.3276G= MANE Select	NP_114432.2:p.Pro1092=