Canonical Allele Identifier: CA2269131020

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683831G= , CM000679.2:g.61683831G=	GRCh38
NC_000017.10:g.59761192G= , CM000679.1:g.59761192G=	GRCh37
NC_000017.9:g.57115974G=	NCBI36
NG_007409.2:g.184729C= , LRG_300:g.184729C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1955C=
ENST00000682453.1:c.3215C=	ENSP00000506943.1:p.Thr1072=
ENST00000682477.1:c.*2641C=	ENSP00000507075.1:n.*2641C=
ENST00000682589.1:n.9092C=
ENST00000682755.1:c.2993C=	ENSP00000507660.1:p.Thr998=
ENST00000682989.1:c.*306C=	ENSP00000507786.1:n.*306C=
ENST00000683039.1:c.3215C=	ENSP00000508303.1:p.Thr1072=
ENST00000683235.1:c.*630C=	ENSP00000507646.1:n.*630C=
ENST00000683535.1:n.1345C=
ENST00000684584.1:c.2378C=	ENSP00000508044.1:p.Thr793=
ENST00000684626.1:n.1461C=
ENST00000684769.1:c.1405C=	ENSP00000507691.1:n.1405C=
ENST00000259008.7:c.3215C= MANE Select	ENSP00000259008.2:p.Thr1072=
ENST00000259008.6:c.3215C=	ENSP00000259008.2:p.Thr1072=
NM_032043.2:c.3215C= , LRG_300t1:c.3215C=	NP_114432.2:p.Thr1072=
XM_011525332.1:c.3275C=	XP_011523634.1:p.Thr1092=
XM_011525333.1:c.3275C=	XP_011523635.1:p.Thr1092=
XM_011525334.1:c.3275C=	XP_011523636.1:p.Thr1092=
XM_011525335.1:c.3215C=	XP_011523637.1:p.Thr1072=
XM_011525336.1:c.3155C=	XP_011523638.1:p.Thr1052=
XM_011525337.1:c.3074C=	XP_011523639.1:p.Thr1025=
XM_011525338.1:c.2792C=	XP_011523640.1:p.Thr931=
XM_011525332.3:c.3275C=	XP_011523634.1:p.Thr1092=
XM_011525333.3:c.3275C=	XP_011523635.1:p.Thr1092=
XM_011525334.2:c.3275C=	XP_011523636.1:p.Thr1092=
XM_011525335.3:c.3215C=	XP_011523637.1:p.Thr1072=
XM_011525336.2:c.3155C=	XP_011523638.1:p.Thr1052=
XM_011525337.2:c.3074C=	XP_011523639.1:p.Thr1025=
XM_011525338.2:c.2792C=	XP_011523640.1:p.Thr931=
XM_017025200.1:c.2732C=	XP_016880689.1:p.Thr911=
XM_017025201.1:c.2732C=	XP_016880690.1:p.Thr911=
XM_017025202.1:c.1361C=	XP_016880691.1:p.Thr454=
XM_017025203.1:c.1361C=	XP_016880692.1:p.Thr454=
NM_032043.3:c.3215C= MANE Select	NP_114432.2:p.Thr1072=