Canonical Allele Identifier: CA2269130980

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683769G= , CM000679.2:g.61683769G=	GRCh38
NC_000017.10:g.59761130G= , CM000679.1:g.59761130G=	GRCh37
NC_000017.9:g.57115912G=	NCBI36
NG_007409.2:g.184791C= , LRG_300:g.184791C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2017C=
ENST00000682453.1:c.3277C=	ENSP00000506943.1:p.Leu1093=
ENST00000682477.1:c.*2703C=	ENSP00000507075.1:n.*2703C=
ENST00000682589.1:n.9154C=
ENST00000682755.1:c.3055C=	ENSP00000507660.1:p.Leu1019=
ENST00000682989.1:c.*368C=	ENSP00000507786.1:n.*368C=
ENST00000683039.1:c.3277C=	ENSP00000508303.1:p.Leu1093=
ENST00000683235.1:c.*692C=	ENSP00000507646.1:n.*692C=
ENST00000683535.1:n.1407C=
ENST00000684584.1:c.2440C=	ENSP00000508044.1:p.Leu814=
ENST00000684626.1:n.1523C=
ENST00000684769.1:c.1467C=	ENSP00000507691.1:n.1467C=
ENST00000259008.7:c.3277C= MANE Select	ENSP00000259008.2:p.Leu1093=
ENST00000259008.6:c.3277C=	ENSP00000259008.2:p.Leu1093=
NM_032043.2:c.3277C= , LRG_300t1:c.3277C=	NP_114432.2:p.Leu1093=
XM_011525332.1:c.3337C=	XP_011523634.1:p.Leu1113=
XM_011525333.1:c.3337C=	XP_011523635.1:p.Leu1113=
XM_011525334.1:c.3337C=	XP_011523636.1:p.Leu1113=
XM_011525335.1:c.3277C=	XP_011523637.1:p.Leu1093=
XM_011525336.1:c.3217C=	XP_011523638.1:p.Leu1073=
XM_011525337.1:c.3136C=	XP_011523639.1:p.Leu1046=
XM_011525338.1:c.2854C=	XP_011523640.1:p.Leu952=
XM_011525332.3:c.3337C=	XP_011523634.1:p.Leu1113=
XM_011525333.3:c.3337C=	XP_011523635.1:p.Leu1113=
XM_011525334.2:c.3337C=	XP_011523636.1:p.Leu1113=
XM_011525335.3:c.3277C=	XP_011523637.1:p.Leu1093=
XM_011525336.2:c.3217C=	XP_011523638.1:p.Leu1073=
XM_011525337.2:c.3136C=	XP_011523639.1:p.Leu1046=
XM_011525338.2:c.2854C=	XP_011523640.1:p.Leu952=
XM_017025200.1:c.2794C=	XP_016880689.1:p.Leu932=
XM_017025201.1:c.2794C=	XP_016880690.1:p.Leu932=
XM_017025202.1:c.1423C=	XP_016880691.1:p.Leu475=
XM_017025203.1:c.1423C=	XP_016880692.1:p.Leu475=
NM_032043.3:c.3277C= MANE Select	NP_114432.2:p.Leu1093=