Canonical Allele Identifier: CA2269130764

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683433T= , CM000679.2:g.61683433T=	GRCh38
NC_000017.10:g.59760794T= , CM000679.1:g.59760794T=	GRCh37
NC_000017.9:g.57115576T=	NCBI36
NG_007409.2:g.185127A= , LRG_300:g.185127A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2353A=
ENST00000682453.1:c.3613A=	ENSP00000506943.1:p.Lys1205=
ENST00000682477.1:c.*3039A=	ENSP00000507075.1:n.*3039A=
ENST00000682589.1:n.9490A=
ENST00000682755.1:c.3391A=	ENSP00000507660.1:p.Lys1131=
ENST00000682989.1:c.*704A=	ENSP00000507786.1:n.*704A=
ENST00000683039.1:c.3613A=	ENSP00000508303.1:p.Lys1205=
ENST00000683235.1:c.*1028A=	ENSP00000507646.1:n.*1028A=
ENST00000683535.1:n.1743A=
ENST00000684584.1:c.2776A=	ENSP00000508044.1:p.Lys926=
ENST00000684626.1:n.1859A=
ENST00000684769.1:c.1803A=	ENSP00000507691.1:n.1803A=
ENST00000259008.7:c.3613A= MANE Select	ENSP00000259008.2:p.Lys1205=
ENST00000259008.6:c.3613A=	ENSP00000259008.2:p.Lys1205=
NM_032043.2:c.3613A= , LRG_300t1:c.3613A=	NP_114432.2:p.Lys1205=
XM_011525332.1:c.3673A=	XP_011523634.1:p.Lys1225=
XM_011525333.1:c.3673A=	XP_011523635.1:p.Lys1225=
XM_011525334.1:c.3673A=	XP_011523636.1:p.Lys1225=
XM_011525335.1:c.3613A=	XP_011523637.1:p.Lys1205=
XM_011525336.1:c.3553A=	XP_011523638.1:p.Lys1185=
XM_011525337.1:c.3472A=	XP_011523639.1:p.Lys1158=
XM_011525338.1:c.3190A=	XP_011523640.1:p.Lys1064=
XM_011525332.3:c.3673A=	XP_011523634.1:p.Lys1225=
XM_011525333.3:c.3673A=	XP_011523635.1:p.Lys1225=
XM_011525334.2:c.3673A=	XP_011523636.1:p.Lys1225=
XM_011525335.3:c.3613A=	XP_011523637.1:p.Lys1205=
XM_011525336.2:c.3553A=	XP_011523638.1:p.Lys1185=
XM_011525337.2:c.3472A=	XP_011523639.1:p.Lys1158=
XM_011525338.2:c.3190A=	XP_011523640.1:p.Lys1064=
XM_017025200.1:c.3130A=	XP_016880689.1:p.Lys1044=
XM_017025201.1:c.3130A=	XP_016880690.1:p.Lys1044=
XM_017025202.1:c.1759A=	XP_016880691.1:p.Lys587=
XM_017025203.1:c.1759A=	XP_016880692.1:p.Lys587=
NM_032043.3:c.3613A= MANE Select	NP_114432.2:p.Lys1205=