Canonical Allele Identifier: CA2269170301

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61780358G= , CM000679.2:g.61780358G=	GRCh38
NC_000017.10:g.59857719G= , CM000679.1:g.59857719G=	GRCh37
NC_000017.9:g.57212501G=	NCBI36
NG_007409.2:g.88202C= , LRG_300:g.88202C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.1420C=	ENSP00000463827.2:n.1420C=
ENST00000584322.2:c.1838C=	ENSP00000463272.2:p.Thr613=
ENST00000682066.1:c.1331C=	ENSP00000507191.1:p.Thr444=
ENST00000682073.1:n.578C=
ENST00000682453.1:c.1838C=	ENSP00000506943.1:p.Thr613=
ENST00000682477.1:c.*1264C=	ENSP00000507075.1:n.*1264C=
ENST00000682589.1:n.4017C=
ENST00000682611.1:c.1331C=	ENSP00000508326.1:p.Thr444=
ENST00000682755.1:c.1616C=	ENSP00000507660.1:p.Thr539=
ENST00000682989.1:c.1838C=	ENSP00000507786.1:p.Thr613=
ENST00000683039.1:c.1838C=	ENSP00000508303.1:p.Thr613=
ENST00000683235.1:c.1838C=	ENSP00000507646.1:p.Thr613=
ENST00000683381.1:c.1838C=	ENSP00000508184.1:p.Thr613=
ENST00000684471.1:n.311C=
ENST00000684584.1:c.1331C=	ENSP00000508044.1:p.Thr444=
ENST00000259008.7:c.1838C= MANE Select	ENSP00000259008.2:p.Thr613=
ENST00000259008.6:c.1838C=	ENSP00000259008.2:p.Thr613=
ENST00000577598.5:c.1838C=	ENSP00000464654.1:p.Thr613=
ENST00000579028.1:c.531C=
NM_032043.2:c.1838C= , LRG_300t1:c.1838C=	NP_114432.2:p.Thr613=
XM_011525332.1:c.1838C=	XP_011523634.1:p.Thr613=
XM_011525333.1:c.1838C=	XP_011523635.1:p.Thr613=
XM_011525334.1:c.1838C=	XP_011523636.1:p.Thr613=
XM_011525335.1:c.1838C=	XP_011523637.1:p.Thr613=
XM_011525336.1:c.1838C=	XP_011523638.1:p.Thr613=
XM_011525337.1:c.1794+482C=	XP_011523639.1:n.1794+482C=
XM_011525338.1:c.1355C=	XP_011523640.1:p.Thr452=
XM_011525339.1:c.1838C=	XP_011523641.1:p.Thr613=
XM_011525340.1:c.1838C=	XP_011523642.1:p.Thr613=
XM_011525341.1:c.1838C=	XP_011523643.1:p.Thr613=
XM_011525332.3:c.1838C=	XP_011523634.1:p.Thr613=
XM_011525333.3:c.1838C=	XP_011523635.1:p.Thr613=
XM_011525334.2:c.1838C=	XP_011523636.1:p.Thr613=
XM_011525335.3:c.1838C=	XP_011523637.1:p.Thr613=
XM_011525336.2:c.1838C=	XP_011523638.1:p.Thr613=
XM_011525337.2:c.1794+482C=	XP_011523639.1:n.1794+482C=
XM_011525338.2:c.1355C=	XP_011523640.1:p.Thr452=
XM_011525339.3:c.1838C=	XP_011523641.1:p.Thr613=
XM_011525340.3:c.1838C=	XP_011523642.1:p.Thr613=
XM_011525341.3:c.1838C=	XP_011523643.1:p.Thr613=
XM_017025200.1:c.1355C=	XP_016880689.1:p.Thr452=
XM_017025201.1:c.1295C=	XP_016880690.1:p.Thr432=
NM_032043.3:c.1838C= MANE Select	NP_114432.2:p.Thr613=