Canonical Allele Identifier: CA501150305

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 530372
• ClinVar RCV Id: RCV001468850 ; RCV002406367
• dbSNP Id: rs1555602134
• MyVariant Identifiers: chr17:g.59857649C>T (hg19) ; chr17:g.61780288C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61780288C>T , CM000679.2:g.61780288C>T	GRCh38
NC_000017.10:g.59857649C>T , CM000679.1:g.59857649C>T	GRCh37
NC_000017.9:g.57212431C>T	NCBI36
NG_007409.2:g.88272G>A , LRG_300:g.88272G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.1490G>A	ENSP00000463827.2:n.1490G>A
ENST00000584322.2:c.1908G>A	ENSP00000463272.2:p.Glu636=
ENST00000682066.1:c.1401G>A	ENSP00000507191.1:p.Glu467=
ENST00000682073.1:n.648G>A
ENST00000682453.1:c.1908G>A	ENSP00000506943.1:p.Glu636=
ENST00000682477.1:c.*1334G>A	ENSP00000507075.1:n.*1334G>A
ENST00000682589.1:n.4087G>A
ENST00000682611.1:c.1401G>A	ENSP00000508326.1:p.Glu467=
ENST00000682755.1:c.1686G>A	ENSP00000507660.1:p.Glu562=
ENST00000682989.1:c.1908G>A	ENSP00000507786.1:p.Glu636=
ENST00000683039.1:c.1908G>A	ENSP00000508303.1:p.Glu636=
ENST00000683235.1:c.1908G>A	ENSP00000507646.1:p.Glu636=
ENST00000683381.1:c.1908G>A	ENSP00000508184.1:p.Glu636=
ENST00000684471.1:n.381G>A
ENST00000684584.1:c.1401G>A	ENSP00000508044.1:p.Glu467=
ENST00000259008.7:c.1908G>A MANE Select	ENSP00000259008.2:p.Glu636=
ENST00000259008.6:c.1908G>A	ENSP00000259008.2:p.Glu636=
ENST00000577598.5:c.1908G>A	ENSP00000464654.1:p.Glu636=
ENST00000579028.1:c.601G>A
NM_032043.2:c.1908G>A , LRG_300t1:c.1908G>A	NP_114432.2:p.Glu636=
XM_011525332.1:c.1908G>A	XP_011523634.1:p.Glu636=
XM_011525333.1:c.1908G>A	XP_011523635.1:p.Glu636=
XM_011525334.1:c.1908G>A	XP_011523636.1:p.Glu636=
XM_011525335.1:c.1908G>A	XP_011523637.1:p.Glu636=
XM_011525336.1:c.1908G>A	XP_011523638.1:p.Glu636=
XM_011525337.1:c.1794+552G>A	XP_011523639.1:n.1794+552G>A
XM_011525338.1:c.1425G>A	XP_011523640.1:p.Glu475=
XM_011525339.1:c.1908G>A	XP_011523641.1:p.Glu636=
XM_011525340.1:c.1908G>A	XP_011523642.1:p.Glu636=
XM_011525341.1:c.1908G>A	XP_011523643.1:p.Glu636=
XM_011525332.3:c.1908G>A	XP_011523634.1:p.Glu636=
XM_011525333.3:c.1908G>A	XP_011523635.1:p.Glu636=
XM_011525334.2:c.1908G>A	XP_011523636.1:p.Glu636=
XM_011525335.3:c.1908G>A	XP_011523637.1:p.Glu636=
XM_011525336.2:c.1908G>A	XP_011523638.1:p.Glu636=
XM_011525337.2:c.1794+552G>A	XP_011523639.1:n.1794+552G>A
XM_011525338.2:c.1425G>A	XP_011523640.1:p.Glu475=
XM_011525339.3:c.1908G>A	XP_011523641.1:p.Glu636=
XM_011525340.3:c.1908G>A	XP_011523642.1:p.Glu636=
XM_011525341.3:c.1908G>A	XP_011523643.1:p.Glu636=
XM_017025200.1:c.1425G>A	XP_016880689.1:p.Glu475=
XM_017025201.1:c.1365G>A	XP_016880690.1:p.Glu455=
XM_017025203.1:c.-53G>A	XP_016880692.1:n.-53G>A
NM_032043.3:c.1908G>A MANE Select	NP_114432.2:p.Glu636=