Canonical Allele Identifier: CA2269131114

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683985G= , CM000679.2:g.61683985G=	GRCh38
NC_000017.10:g.59761346G= , CM000679.1:g.59761346G=	GRCh37
NC_000017.9:g.57116128G=	NCBI36
NG_007409.2:g.184575C= , LRG_300:g.184575C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682073.1:n.1801C=
ENST00000682453.1:c.3061C=	ENSP00000506943.1:p.Pro1021=
ENST00000682477.1:c.*2487C=	ENSP00000507075.1:n.*2487C=
ENST00000682589.1:n.8938C=
ENST00000682755.1:c.2839C=	ENSP00000507660.1:p.Pro947=
ENST00000682989.1:c.*152C=	ENSP00000507786.1:n.*152C=
ENST00000683039.1:c.3061C=	ENSP00000508303.1:p.Pro1021=
ENST00000683235.1:c.*476C=	ENSP00000507646.1:n.*476C=
ENST00000683535.1:n.1191C=
ENST00000684584.1:c.2224C=	ENSP00000508044.1:p.Pro742=
ENST00000684626.1:n.1307C=
ENST00000684769.1:c.1251C=	ENSP00000507691.1:n.1251C=
ENST00000259008.7:c.3061C= MANE Select	ENSP00000259008.2:p.Pro1021=
ENST00000259008.6:c.3061C=	ENSP00000259008.2:p.Pro1021=
NM_032043.2:c.3061C= , LRG_300t1:c.3061C=	NP_114432.2:p.Pro1021=
XM_011525332.1:c.3121C=	XP_011523634.1:p.Pro1041=
XM_011525333.1:c.3121C=	XP_011523635.1:p.Pro1041=
XM_011525334.1:c.3121C=	XP_011523636.1:p.Pro1041=
XM_011525335.1:c.3061C=	XP_011523637.1:p.Pro1021=
XM_011525336.1:c.3001C=	XP_011523638.1:p.Pro1001=
XM_011525337.1:c.2920C=	XP_011523639.1:p.Pro974=
XM_011525338.1:c.2638C=	XP_011523640.1:p.Pro880=
XM_011525332.3:c.3121C=	XP_011523634.1:p.Pro1041=
XM_011525333.3:c.3121C=	XP_011523635.1:p.Pro1041=
XM_011525334.2:c.3121C=	XP_011523636.1:p.Pro1041=
XM_011525335.3:c.3061C=	XP_011523637.1:p.Pro1021=
XM_011525336.2:c.3001C=	XP_011523638.1:p.Pro1001=
XM_011525337.2:c.2920C=	XP_011523639.1:p.Pro974=
XM_011525338.2:c.2638C=	XP_011523640.1:p.Pro880=
XM_017025200.1:c.2578C=	XP_016880689.1:p.Pro860=
XM_017025201.1:c.2578C=	XP_016880690.1:p.Pro860=
XM_017025202.1:c.1207C=	XP_016880691.1:p.Pro403=
XM_017025203.1:c.1207C=	XP_016880692.1:p.Pro403=
NM_032043.3:c.3061C= MANE Select	NP_114432.2:p.Pro1021=