Canonical Allele Identifier: CA2269131012

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683816A= , CM000679.2:g.61683816A=	GRCh38
NC_000017.10:g.59761177A= , CM000679.1:g.59761177A=	GRCh37
NC_000017.9:g.57115959A=	NCBI36
NG_007409.2:g.184744T= , LRG_300:g.184744T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1970T=
ENST00000682453.1:c.3230T=	ENSP00000506943.1:p.Leu1077=
ENST00000682477.1:c.*2656T=	ENSP00000507075.1:n.*2656T=
ENST00000682589.1:n.9107T=
ENST00000682755.1:c.3008T=	ENSP00000507660.1:p.Leu1003=
ENST00000682989.1:c.*321T=	ENSP00000507786.1:n.*321T=
ENST00000683039.1:c.3230T=	ENSP00000508303.1:p.Leu1077=
ENST00000683235.1:c.*645T=	ENSP00000507646.1:n.*645T=
ENST00000683535.1:n.1360T=
ENST00000684584.1:c.2393T=	ENSP00000508044.1:p.Leu798=
ENST00000684626.1:n.1476T=
ENST00000684769.1:c.1420T=	ENSP00000507691.1:n.1420T=
ENST00000259008.7:c.3230T= MANE Select	ENSP00000259008.2:p.Leu1077=
ENST00000259008.6:c.3230T=	ENSP00000259008.2:p.Leu1077=
NM_032043.2:c.3230T= , LRG_300t1:c.3230T=	NP_114432.2:p.Leu1077=
XM_011525332.1:c.3290T=	XP_011523634.1:p.Leu1097=
XM_011525333.1:c.3290T=	XP_011523635.1:p.Leu1097=
XM_011525334.1:c.3290T=	XP_011523636.1:p.Leu1097=
XM_011525335.1:c.3230T=	XP_011523637.1:p.Leu1077=
XM_011525336.1:c.3170T=	XP_011523638.1:p.Leu1057=
XM_011525337.1:c.3089T=	XP_011523639.1:p.Leu1030=
XM_011525338.1:c.2807T=	XP_011523640.1:p.Leu936=
XM_011525332.3:c.3290T=	XP_011523634.1:p.Leu1097=
XM_011525333.3:c.3290T=	XP_011523635.1:p.Leu1097=
XM_011525334.2:c.3290T=	XP_011523636.1:p.Leu1097=
XM_011525335.3:c.3230T=	XP_011523637.1:p.Leu1077=
XM_011525336.2:c.3170T=	XP_011523638.1:p.Leu1057=
XM_011525337.2:c.3089T=	XP_011523639.1:p.Leu1030=
XM_011525338.2:c.2807T=	XP_011523640.1:p.Leu936=
XM_017025200.1:c.2747T=	XP_016880689.1:p.Leu916=
XM_017025201.1:c.2747T=	XP_016880690.1:p.Leu916=
XM_017025202.1:c.1376T=	XP_016880691.1:p.Leu459=
XM_017025203.1:c.1376T=	XP_016880692.1:p.Leu459=
NM_032043.3:c.3230T= MANE Select	NP_114432.2:p.Leu1077=