Canonical Allele Identifier: CA2269130898

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683639A= , CM000679.2:g.61683639A=	GRCh38
NC_000017.10:g.59761000A= , CM000679.1:g.59761000A=	GRCh37
NC_000017.9:g.57115782A=	NCBI36
NG_007409.2:g.184921T= , LRG_300:g.184921T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2147T=
ENST00000682453.1:c.3407T=	ENSP00000506943.1:p.Leu1136=
ENST00000682477.1:c.*2833T=	ENSP00000507075.1:n.*2833T=
ENST00000682589.1:n.9284T=
ENST00000682755.1:c.3185T=	ENSP00000507660.1:p.Leu1062=
ENST00000682989.1:c.*498T=	ENSP00000507786.1:n.*498T=
ENST00000683039.1:c.3407T=	ENSP00000508303.1:p.Leu1136=
ENST00000683235.1:c.*822T=	ENSP00000507646.1:n.*822T=
ENST00000683535.1:n.1537T=
ENST00000684584.1:c.2570T=	ENSP00000508044.1:p.Leu857=
ENST00000684626.1:n.1653T=
ENST00000684769.1:c.1597T=	ENSP00000507691.1:n.1597T=
ENST00000259008.7:c.3407T= MANE Select	ENSP00000259008.2:p.Leu1136=
ENST00000259008.6:c.3407T=	ENSP00000259008.2:p.Leu1136=
NM_032043.2:c.3407T= , LRG_300t1:c.3407T=	NP_114432.2:p.Leu1136=
XM_011525332.1:c.3467T=	XP_011523634.1:p.Leu1156=
XM_011525333.1:c.3467T=	XP_011523635.1:p.Leu1156=
XM_011525334.1:c.3467T=	XP_011523636.1:p.Leu1156=
XM_011525335.1:c.3407T=	XP_011523637.1:p.Leu1136=
XM_011525336.1:c.3347T=	XP_011523638.1:p.Leu1116=
XM_011525337.1:c.3266T=	XP_011523639.1:p.Leu1089=
XM_011525338.1:c.2984T=	XP_011523640.1:p.Leu995=
XM_011525332.3:c.3467T=	XP_011523634.1:p.Leu1156=
XM_011525333.3:c.3467T=	XP_011523635.1:p.Leu1156=
XM_011525334.2:c.3467T=	XP_011523636.1:p.Leu1156=
XM_011525335.3:c.3407T=	XP_011523637.1:p.Leu1136=
XM_011525336.2:c.3347T=	XP_011523638.1:p.Leu1116=
XM_011525337.2:c.3266T=	XP_011523639.1:p.Leu1089=
XM_011525338.2:c.2984T=	XP_011523640.1:p.Leu995=
XM_017025200.1:c.2924T=	XP_016880689.1:p.Leu975=
XM_017025201.1:c.2924T=	XP_016880690.1:p.Leu975=
XM_017025202.1:c.1553T=	XP_016880691.1:p.Leu518=
XM_017025203.1:c.1553T=	XP_016880692.1:p.Leu518=
NM_032043.3:c.3407T= MANE Select	NP_114432.2:p.Leu1136=