Canonical Allele Identifier: CA2269130847

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683553T= , CM000679.2:g.61683553T=	GRCh38
NC_000017.10:g.59760914T= , CM000679.1:g.59760914T=	GRCh37
NC_000017.9:g.57115696T=	NCBI36
NG_007409.2:g.185007A= , LRG_300:g.185007A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2233A=
ENST00000682453.1:c.3493A=	ENSP00000506943.1:p.Ile1165=
ENST00000682477.1:c.*2919A=	ENSP00000507075.1:n.*2919A=
ENST00000682589.1:n.9370A=
ENST00000682755.1:c.3271A=	ENSP00000507660.1:p.Ile1091=
ENST00000682989.1:c.*584A=	ENSP00000507786.1:n.*584A=
ENST00000683039.1:c.3493A=	ENSP00000508303.1:p.Ile1165=
ENST00000683235.1:c.*908A=	ENSP00000507646.1:n.*908A=
ENST00000683535.1:n.1623A=
ENST00000684584.1:c.2656A=	ENSP00000508044.1:p.Ile886=
ENST00000684626.1:n.1739A=
ENST00000684769.1:c.1683A=	ENSP00000507691.1:n.1683A=
ENST00000259008.7:c.3493A= MANE Select	ENSP00000259008.2:p.Ile1165=
ENST00000259008.6:c.3493A=	ENSP00000259008.2:p.Ile1165=
NM_032043.2:c.3493A= , LRG_300t1:c.3493A=	NP_114432.2:p.Ile1165=
XM_011525332.1:c.3553A=	XP_011523634.1:p.Ile1185=
XM_011525333.1:c.3553A=	XP_011523635.1:p.Ile1185=
XM_011525334.1:c.3553A=	XP_011523636.1:p.Ile1185=
XM_011525335.1:c.3493A=	XP_011523637.1:p.Ile1165=
XM_011525336.1:c.3433A=	XP_011523638.1:p.Ile1145=
XM_011525337.1:c.3352A=	XP_011523639.1:p.Ile1118=
XM_011525338.1:c.3070A=	XP_011523640.1:p.Ile1024=
XM_011525332.3:c.3553A=	XP_011523634.1:p.Ile1185=
XM_011525333.3:c.3553A=	XP_011523635.1:p.Ile1185=
XM_011525334.2:c.3553A=	XP_011523636.1:p.Ile1185=
XM_011525335.3:c.3493A=	XP_011523637.1:p.Ile1165=
XM_011525336.2:c.3433A=	XP_011523638.1:p.Ile1145=
XM_011525337.2:c.3352A=	XP_011523639.1:p.Ile1118=
XM_011525338.2:c.3070A=	XP_011523640.1:p.Ile1024=
XM_017025200.1:c.3010A=	XP_016880689.1:p.Ile1004=
XM_017025201.1:c.3010A=	XP_016880690.1:p.Ile1004=
XM_017025202.1:c.1639A=	XP_016880691.1:p.Ile547=
XM_017025203.1:c.1639A=	XP_016880692.1:p.Ile547=
NM_032043.3:c.3493A= MANE Select	NP_114432.2:p.Ile1165=