Canonical Allele Identifier: CA2580094530

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 2030175
• ClinVar RCV Id: RCV002881192
• dbSNP Id: rs2145134648

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61784267del , CM000679.2:g.61784267del	GRCh38
NC_000017.10:g.59861628del , CM000679.1:g.59861628del	GRCh37
NC_000017.9:g.57216410del	NCBI36
NG_007409.2:g.84294del , LRG_300:g.84294del

Transcript Alleles

HGVS	Amino-acid change
ENST00000579028.2:c.1121+4del	ENSP00000463827.2:n.1121+4del
ENST00000584322.2:c.1628+4del	ENSP00000463272.2:n.1628+4del
ENST00000682066.1:c.1121+4del	ENSP00000507191.1:n.1121+4del
ENST00000682073.1:n.368+4del
ENST00000682453.1:c.1628+4del	ENSP00000506943.1:n.1628+4del
ENST00000682477.1:c.*1054+4del	ENSP00000507075.1:n.*1054+4del
ENST00000682589.1:n.3369+4del
ENST00000682611.1:c.1121+4del	ENSP00000508326.1:n.1121+4del
ENST00000682755.1:c.1406+4del	ENSP00000507660.1:n.1406+4del
ENST00000682989.1:c.1628+4del	ENSP00000507786.1:n.1628+4del
ENST00000683039.1:c.1628+4del	ENSP00000508303.1:n.1628+4del
ENST00000683235.1:c.1628+4del	ENSP00000507646.1:n.1628+4del
ENST00000683381.1:c.1628+4del	ENSP00000508184.1:n.1628+4del
ENST00000684584.1:c.1121+4del	ENSP00000508044.1:n.1121+4del
ENST00000259008.7:c.1628+4del MANE Select	ENSP00000259008.2:n.1628+4del
ENST00000259008.6:c.1628+4del	ENSP00000259008.2:n.1628+4del
ENST00000577598.5:c.1628+4del	ENSP00000464654.1:n.1628+4del
ENST00000579028.1:c.232+4del
NM_032043.2:c.1628+4del , LRG_300t1:c.1628+4del	NP_114432.2:n.1628+4del
XM_011525332.1:c.1628+4del	XP_011523634.1:n.1628+4del
XM_011525333.1:c.1628+4del	XP_011523635.1:n.1628+4del
XM_011525334.1:c.1628+4del	XP_011523636.1:n.1628+4del
XM_011525335.1:c.1628+4del	XP_011523637.1:n.1628+4del
XM_011525336.1:c.1628+4del	XP_011523638.1:n.1628+4del
XM_011525337.1:c.1628+4del	XP_011523639.1:n.1628+4del
XM_011525338.1:c.1145+4del	XP_011523640.1:n.1145+4del
XM_011525339.1:c.1628+4del	XP_011523641.1:n.1628+4del
XM_011525340.1:c.1628+4del	XP_011523642.1:n.1628+4del
XM_011525341.1:c.1628+4del	XP_011523643.1:n.1628+4del
XM_011525332.3:c.1628+4del	XP_011523634.1:n.1628+4del
XM_011525333.3:c.1628+4del	XP_011523635.1:n.1628+4del
XM_011525334.2:c.1628+4del	XP_011523636.1:n.1628+4del
XM_011525335.3:c.1628+4del	XP_011523637.1:n.1628+4del
XM_011525336.2:c.1628+4del	XP_011523638.1:n.1628+4del
XM_011525337.2:c.1628+4del	XP_011523639.1:n.1628+4del
XM_011525338.2:c.1145+4del	XP_011523640.1:n.1145+4del
XM_011525339.3:c.1628+4del	XP_011523641.1:n.1628+4del
XM_011525340.3:c.1628+4del	XP_011523642.1:n.1628+4del
XM_011525341.3:c.1628+4del	XP_011523643.1:n.1628+4del
XM_017025200.1:c.1145+4del	XP_016880689.1:n.1145+4del
XM_017025201.1:c.1085+4del	XP_016880690.1:n.1085+4del
NM_032043.3:c.1628+4del MANE Select	NP_114432.2:n.1628+4del