Canonical Allele Identifier: CA289734

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61743106A>G , CM000679.2:g.61743106A>G	GRCh38
NC_000017.10:g.59820467A>G , CM000679.1:g.59820467A>G	GRCh37
NC_000017.9:g.57175249A>G	NCBI36
NG_007409.2:g.125454T>C , LRG_300:g.125454T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000584322.2:c.2286T>C	ENSP00000463272.2:p.Arg762=
ENST00000682066.1:c.2416T>C	ENSP00000507191.1:n.2416T>C
ENST00000682073.1:n.1026T>C
ENST00000682433.1:n.1365T>C
ENST00000682453.1:c.2286T>C	ENSP00000506943.1:p.Arg762=
ENST00000682477.1:c.*1712T>C	ENSP00000507075.1:n.*1712T>C
ENST00000682589.1:n.8163T>C
ENST00000682755.1:c.2064T>C	ENSP00000507660.1:p.Arg688=
ENST00000682989.1:c.2286T>C	ENSP00000507786.1:p.Arg762=
ENST00000683039.1:c.2286T>C	ENSP00000508303.1:p.Arg762=
ENST00000683235.1:c.2286T>C	ENSP00000507646.1:p.Arg762=
ENST00000683381.1:c.2346T>C	ENSP00000508184.1:p.Arg782=
ENST00000683535.1:n.416T>C
ENST00000684471.1:n.699T>C
ENST00000684584.1:c.1779T>C	ENSP00000508044.1:p.Arg593=
ENST00000684769.1:c.351T>C	ENSP00000507691.1:p.Arg117=
ENST00000259008.7:c.2286T>C MANE Select	ENSP00000259008.2:p.Arg762=
ENST00000259008.6:c.2286T>C	ENSP00000259008.2:p.Arg762=
ENST00000577598.5:c.2286T>C	ENSP00000464654.1:p.Arg762=
ENST00000584322.1:c.269T>C
NM_032043.2:c.2286T>C , LRG_300t1:c.2286T>C	NP_114432.2:p.Arg762=
XM_011525332.1:c.2346T>C	XP_011523634.1:p.Arg782=
XM_011525333.1:c.2346T>C	XP_011523635.1:p.Arg782=
XM_011525334.1:c.2346T>C	XP_011523636.1:p.Arg782=
XM_011525335.1:c.2286T>C	XP_011523637.1:p.Arg762=
XM_011525336.1:c.2226T>C	XP_011523638.1:p.Arg742=
XM_011525337.1:c.2145T>C	XP_011523639.1:p.Arg715=
XM_011525338.1:c.1863T>C	XP_011523640.1:p.Arg621=
XM_011525339.1:c.2346T>C	XP_011523641.1:p.Arg782=
XM_011525340.1:c.2346T>C	XP_011523642.1:p.Arg782=
XR_934894.1:n.524-1075A>G
XM_011525332.3:c.2346T>C	XP_011523634.1:p.Arg782=
XM_011525333.3:c.2346T>C	XP_011523635.1:p.Arg782=
XM_011525334.2:c.2346T>C	XP_011523636.1:p.Arg782=
XM_011525335.3:c.2286T>C	XP_011523637.1:p.Arg762=
XM_011525336.2:c.2226T>C	XP_011523638.1:p.Arg742=
XM_011525337.2:c.2145T>C	XP_011523639.1:p.Arg715=
XM_011525338.2:c.1863T>C	XP_011523640.1:p.Arg621=
XM_011525339.3:c.2346T>C	XP_011523641.1:p.Arg782=
XM_011525340.3:c.2346T>C	XP_011523642.1:p.Arg782=
XM_017025200.1:c.1803T>C	XP_016880689.1:p.Arg601=
XM_017025201.1:c.1803T>C	XP_016880690.1:p.Arg601=
XM_017025202.1:c.432T>C	XP_016880691.1:p.Arg144=
XM_017025203.1:c.432T>C	XP_016880692.1:p.Arg144=
NM_032043.3:c.2286T>C MANE Select	NP_114432.2:p.Arg762=