Canonical Allele Identifier: CA2269131090

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683953A= , CM000679.2:g.61683953A=	GRCh38
NC_000017.10:g.59761314A= , CM000679.1:g.59761314A=	GRCh37
NC_000017.9:g.57116096A=	NCBI36
NG_007409.2:g.184607T= , LRG_300:g.184607T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1833T=
ENST00000682453.1:c.3093T=	ENSP00000506943.1:p.Ser1031=
ENST00000682477.1:c.*2519T=	ENSP00000507075.1:n.*2519T=
ENST00000682589.1:n.8970T=
ENST00000682755.1:c.2871T=	ENSP00000507660.1:p.Ser957=
ENST00000682989.1:c.*184T=	ENSP00000507786.1:n.*184T=
ENST00000683039.1:c.3093T=	ENSP00000508303.1:p.Ser1031=
ENST00000683235.1:c.*508T=	ENSP00000507646.1:n.*508T=
ENST00000683535.1:n.1223T=
ENST00000684584.1:c.2256T=	ENSP00000508044.1:p.Ser752=
ENST00000684626.1:n.1339T=
ENST00000684769.1:c.1283T=	ENSP00000507691.1:n.1283T=
ENST00000259008.7:c.3093T= MANE Select	ENSP00000259008.2:p.Ser1031=
ENST00000259008.6:c.3093T=	ENSP00000259008.2:p.Ser1031=
NM_032043.2:c.3093T= , LRG_300t1:c.3093T=	NP_114432.2:p.Ser1031=
XM_011525332.1:c.3153T=	XP_011523634.1:p.Ser1051=
XM_011525333.1:c.3153T=	XP_011523635.1:p.Ser1051=
XM_011525334.1:c.3153T=	XP_011523636.1:p.Ser1051=
XM_011525335.1:c.3093T=	XP_011523637.1:p.Ser1031=
XM_011525336.1:c.3033T=	XP_011523638.1:p.Ser1011=
XM_011525337.1:c.2952T=	XP_011523639.1:p.Ser984=
XM_011525338.1:c.2670T=	XP_011523640.1:p.Ser890=
XM_011525332.3:c.3153T=	XP_011523634.1:p.Ser1051=
XM_011525333.3:c.3153T=	XP_011523635.1:p.Ser1051=
XM_011525334.2:c.3153T=	XP_011523636.1:p.Ser1051=
XM_011525335.3:c.3093T=	XP_011523637.1:p.Ser1031=
XM_011525336.2:c.3033T=	XP_011523638.1:p.Ser1011=
XM_011525337.2:c.2952T=	XP_011523639.1:p.Ser984=
XM_011525338.2:c.2670T=	XP_011523640.1:p.Ser890=
XM_017025200.1:c.2610T=	XP_016880689.1:p.Ser870=
XM_017025201.1:c.2610T=	XP_016880690.1:p.Ser870=
XM_017025202.1:c.1239T=	XP_016880691.1:p.Ser413=
XM_017025203.1:c.1239T=	XP_016880692.1:p.Ser413=
NM_032043.3:c.3093T= MANE Select	NP_114432.2:p.Ser1031=