Canonical Allele Identifier: CA2269130913

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683660G= , CM000679.2:g.61683660G=	GRCh38
NC_000017.10:g.59761021G= , CM000679.1:g.59761021G=	GRCh37
NC_000017.9:g.57115803G=	NCBI36
NG_007409.2:g.184900C= , LRG_300:g.184900C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2126C=
ENST00000682453.1:c.3386C=	ENSP00000506943.1:p.Ser1129=
ENST00000682477.1:c.*2812C=	ENSP00000507075.1:n.*2812C=
ENST00000682589.1:n.9263C=
ENST00000682755.1:c.3164C=	ENSP00000507660.1:p.Ser1055=
ENST00000682989.1:c.*477C=	ENSP00000507786.1:n.*477C=
ENST00000683039.1:c.3386C=	ENSP00000508303.1:p.Ser1129=
ENST00000683235.1:c.*801C=	ENSP00000507646.1:n.*801C=
ENST00000683535.1:n.1516C=
ENST00000684584.1:c.2549C=	ENSP00000508044.1:p.Ser850=
ENST00000684626.1:n.1632C=
ENST00000684769.1:c.1576C=	ENSP00000507691.1:n.1576C=
ENST00000259008.7:c.3386C= MANE Select	ENSP00000259008.2:p.Ser1129=
ENST00000259008.6:c.3386C=	ENSP00000259008.2:p.Ser1129=
NM_032043.2:c.3386C= , LRG_300t1:c.3386C=	NP_114432.2:p.Ser1129=
XM_011525332.1:c.3446C=	XP_011523634.1:p.Ser1149=
XM_011525333.1:c.3446C=	XP_011523635.1:p.Ser1149=
XM_011525334.1:c.3446C=	XP_011523636.1:p.Ser1149=
XM_011525335.1:c.3386C=	XP_011523637.1:p.Ser1129=
XM_011525336.1:c.3326C=	XP_011523638.1:p.Ser1109=
XM_011525337.1:c.3245C=	XP_011523639.1:p.Ser1082=
XM_011525338.1:c.2963C=	XP_011523640.1:p.Ser988=
XM_011525332.3:c.3446C=	XP_011523634.1:p.Ser1149=
XM_011525333.3:c.3446C=	XP_011523635.1:p.Ser1149=
XM_011525334.2:c.3446C=	XP_011523636.1:p.Ser1149=
XM_011525335.3:c.3386C=	XP_011523637.1:p.Ser1129=
XM_011525336.2:c.3326C=	XP_011523638.1:p.Ser1109=
XM_011525337.2:c.3245C=	XP_011523639.1:p.Ser1082=
XM_011525338.2:c.2963C=	XP_011523640.1:p.Ser988=
XM_017025200.1:c.2903C=	XP_016880689.1:p.Ser968=
XM_017025201.1:c.2903C=	XP_016880690.1:p.Ser968=
XM_017025202.1:c.1532C=	XP_016880691.1:p.Ser511=
XM_017025203.1:c.1532C=	XP_016880692.1:p.Ser511=
NM_032043.3:c.3386C= MANE Select	NP_114432.2:p.Ser1129=