Canonical Allele Identifier: CA2269130960

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683739T= , CM000679.2:g.61683739T=	GRCh38
NC_000017.10:g.59761100T= , CM000679.1:g.59761100T=	GRCh37
NC_000017.9:g.57115882T=	NCBI36
NG_007409.2:g.184821A= , LRG_300:g.184821A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2047A=
ENST00000682453.1:c.3307A=	ENSP00000506943.1:p.Ile1103=
ENST00000682477.1:c.*2733A=	ENSP00000507075.1:n.*2733A=
ENST00000682589.1:n.9184A=
ENST00000682755.1:c.3085A=	ENSP00000507660.1:p.Ile1029=
ENST00000682989.1:c.*398A=	ENSP00000507786.1:n.*398A=
ENST00000683039.1:c.3307A=	ENSP00000508303.1:p.Ile1103=
ENST00000683235.1:c.*722A=	ENSP00000507646.1:n.*722A=
ENST00000683535.1:n.1437A=
ENST00000684584.1:c.2470A=	ENSP00000508044.1:p.Ile824=
ENST00000684626.1:n.1553A=
ENST00000684769.1:c.1497A=	ENSP00000507691.1:n.1497A=
ENST00000259008.7:c.3307A= MANE Select	ENSP00000259008.2:p.Ile1103=
ENST00000259008.6:c.3307A=	ENSP00000259008.2:p.Ile1103=
NM_032043.2:c.3307A= , LRG_300t1:c.3307A=	NP_114432.2:p.Ile1103=
XM_011525332.1:c.3367A=	XP_011523634.1:p.Ile1123=
XM_011525333.1:c.3367A=	XP_011523635.1:p.Ile1123=
XM_011525334.1:c.3367A=	XP_011523636.1:p.Ile1123=
XM_011525335.1:c.3307A=	XP_011523637.1:p.Ile1103=
XM_011525336.1:c.3247A=	XP_011523638.1:p.Ile1083=
XM_011525337.1:c.3166A=	XP_011523639.1:p.Ile1056=
XM_011525338.1:c.2884A=	XP_011523640.1:p.Ile962=
XM_011525332.3:c.3367A=	XP_011523634.1:p.Ile1123=
XM_011525333.3:c.3367A=	XP_011523635.1:p.Ile1123=
XM_011525334.2:c.3367A=	XP_011523636.1:p.Ile1123=
XM_011525335.3:c.3307A=	XP_011523637.1:p.Ile1103=
XM_011525336.2:c.3247A=	XP_011523638.1:p.Ile1083=
XM_011525337.2:c.3166A=	XP_011523639.1:p.Ile1056=
XM_011525338.2:c.2884A=	XP_011523640.1:p.Ile962=
XM_017025200.1:c.2824A=	XP_016880689.1:p.Ile942=
XM_017025201.1:c.2824A=	XP_016880690.1:p.Ile942=
XM_017025202.1:c.1453A=	XP_016880691.1:p.Ile485=
XM_017025203.1:c.1453A=	XP_016880692.1:p.Ile485=
NM_032043.3:c.3307A= MANE Select	NP_114432.2:p.Ile1103=