Canonical Allele Identifier: CA2269178615

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61799103A= , CM000679.2:g.61799103A=	GRCh38
NC_000017.10:g.59876464A= , CM000679.1:g.59876464A=	GRCh37
NC_000017.9:g.57231246A=	NCBI36
NG_007409.2:g.69457T= , LRG_300:g.69457T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.830T=	ENSP00000463827.2:p.Ile277=
ENST00000584322.2:c.1337T=	ENSP00000463272.2:p.Ile446=
ENST00000682066.1:c.830T=	ENSP00000507191.1:p.Ile277=
ENST00000682453.1:c.1337T=	ENSP00000506943.1:p.Ile446=
ENST00000682477.1:c.1337T=	ENSP00000507075.1:p.Ile446=
ENST00000682589.1:n.3078T=
ENST00000682611.1:c.830T=	ENSP00000508326.1:p.Ile277=
ENST00000682755.1:c.1115T=	ENSP00000507660.1:p.Ile372=
ENST00000682989.1:c.1337T=	ENSP00000507786.1:p.Ile446=
ENST00000683039.1:c.1337T=	ENSP00000508303.1:p.Ile446=
ENST00000683235.1:c.1337T=	ENSP00000507646.1:p.Ile446=
ENST00000683381.1:c.1337T=	ENSP00000508184.1:p.Ile446=
ENST00000683692.1:c.915T=	ENSP00000507964.1:n.915T=
ENST00000684584.1:c.830T=	ENSP00000508044.1:p.Ile277=
ENST00000259008.7:c.1337T= MANE Select	ENSP00000259008.2:p.Ile446=
ENST00000259008.6:c.1337T=	ENSP00000259008.2:p.Ile446=
ENST00000577598.5:c.1337T=	ENSP00000464654.1:p.Ile446=
NM_032043.2:c.1337T= , LRG_300t1:c.1337T=	NP_114432.2:p.Ile446=
XM_011525332.1:c.1337T=	XP_011523634.1:p.Ile446=
XM_011525333.1:c.1337T=	XP_011523635.1:p.Ile446=
XM_011525334.1:c.1337T=	XP_011523636.1:p.Ile446=
XM_011525335.1:c.1337T=	XP_011523637.1:p.Ile446=
XM_011525336.1:c.1337T=	XP_011523638.1:p.Ile446=
XM_011525337.1:c.1337T=	XP_011523639.1:p.Ile446=
XM_011525338.1:c.854T=	XP_011523640.1:p.Ile285=
XM_011525339.1:c.1337T=	XP_011523641.1:p.Ile446=
XM_011525340.1:c.1337T=	XP_011523642.1:p.Ile446=
XM_011525341.1:c.1337T=	XP_011523643.1:p.Ile446=
XM_011525332.3:c.1337T=	XP_011523634.1:p.Ile446=
XM_011525333.3:c.1337T=	XP_011523635.1:p.Ile446=
XM_011525334.2:c.1337T=	XP_011523636.1:p.Ile446=
XM_011525335.3:c.1337T=	XP_011523637.1:p.Ile446=
XM_011525336.2:c.1337T=	XP_011523638.1:p.Ile446=
XM_011525337.2:c.1337T=	XP_011523639.1:p.Ile446=
XM_011525338.2:c.854T=	XP_011523640.1:p.Ile285=
XM_011525339.3:c.1337T=	XP_011523641.1:p.Ile446=
XM_011525340.3:c.1337T=	XP_011523642.1:p.Ile446=
XM_011525341.3:c.1337T=	XP_011523643.1:p.Ile446=
XM_017025200.1:c.854T=	XP_016880689.1:p.Ile285=
XM_017025201.1:c.794T=	XP_016880690.1:p.Ile265=
NM_032043.3:c.1337T= MANE Select	NP_114432.2:p.Ile446=