Canonical Allele Identifier: CA2269130833

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683523T= , CM000679.2:g.61683523T=	GRCh38
NC_000017.10:g.59760884T= , CM000679.1:g.59760884T=	GRCh37
NC_000017.9:g.57115666T=	NCBI36
NG_007409.2:g.185037A= , LRG_300:g.185037A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2263A=
ENST00000682453.1:c.3523A=	ENSP00000506943.1:p.Thr1175=
ENST00000682477.1:c.*2949A=	ENSP00000507075.1:n.*2949A=
ENST00000682589.1:n.9400A=
ENST00000682755.1:c.3301A=	ENSP00000507660.1:p.Thr1101=
ENST00000682989.1:c.*614A=	ENSP00000507786.1:n.*614A=
ENST00000683039.1:c.3523A=	ENSP00000508303.1:p.Thr1175=
ENST00000683235.1:c.*938A=	ENSP00000507646.1:n.*938A=
ENST00000683535.1:n.1653A=
ENST00000684584.1:c.2686A=	ENSP00000508044.1:p.Thr896=
ENST00000684626.1:n.1769A=
ENST00000684769.1:c.1713A=	ENSP00000507691.1:n.1713A=
ENST00000259008.7:c.3523A= MANE Select	ENSP00000259008.2:p.Thr1175=
ENST00000259008.6:c.3523A=	ENSP00000259008.2:p.Thr1175=
NM_032043.2:c.3523A= , LRG_300t1:c.3523A=	NP_114432.2:p.Thr1175=
XM_011525332.1:c.3583A=	XP_011523634.1:p.Thr1195=
XM_011525333.1:c.3583A=	XP_011523635.1:p.Thr1195=
XM_011525334.1:c.3583A=	XP_011523636.1:p.Thr1195=
XM_011525335.1:c.3523A=	XP_011523637.1:p.Thr1175=
XM_011525336.1:c.3463A=	XP_011523638.1:p.Thr1155=
XM_011525337.1:c.3382A=	XP_011523639.1:p.Thr1128=
XM_011525338.1:c.3100A=	XP_011523640.1:p.Thr1034=
XM_011525332.3:c.3583A=	XP_011523634.1:p.Thr1195=
XM_011525333.3:c.3583A=	XP_011523635.1:p.Thr1195=
XM_011525334.2:c.3583A=	XP_011523636.1:p.Thr1195=
XM_011525335.3:c.3523A=	XP_011523637.1:p.Thr1175=
XM_011525336.2:c.3463A=	XP_011523638.1:p.Thr1155=
XM_011525337.2:c.3382A=	XP_011523639.1:p.Thr1128=
XM_011525338.2:c.3100A=	XP_011523640.1:p.Thr1034=
XM_017025200.1:c.3040A=	XP_016880689.1:p.Thr1014=
XM_017025201.1:c.3040A=	XP_016880690.1:p.Thr1014=
XM_017025202.1:c.1669A=	XP_016880691.1:p.Thr557=
XM_017025203.1:c.1669A=	XP_016880692.1:p.Thr557=
NM_032043.3:c.3523A= MANE Select	NP_114432.2:p.Thr1175=