Canonical Allele Identifier: CA400480177

Gene: BRIP1

Linked Data

• dbSNP Id: rs2145080833
• MyVariant Identifiers: chr17:g.59857737A>T (hg19) ; chr17:g.61780376A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61780376A>T , CM000679.2:g.61780376A>T	GRCh38
NC_000017.10:g.59857737A>T , CM000679.1:g.59857737A>T	GRCh37
NC_000017.9:g.57212519A>T	NCBI36
NG_007409.2:g.88184T>A , LRG_300:g.88184T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.1402T>A	ENSP00000463827.2:n.1402T>A
ENST00000584322.2:c.1820T>A	ENSP00000463272.2:p.Val607Asp
ENST00000682066.1:c.1313T>A	ENSP00000507191.1:p.Val438Asp
ENST00000682073.1:n.560T>A
ENST00000682453.1:c.1820T>A	ENSP00000506943.1:p.Val607Asp
ENST00000682477.1:c.*1246T>A	ENSP00000507075.1:n.*1246T>A
ENST00000682589.1:n.3999T>A
ENST00000682611.1:c.1313T>A	ENSP00000508326.1:p.Val438Asp
ENST00000682755.1:c.1598T>A	ENSP00000507660.1:p.Val533Asp
ENST00000682989.1:c.1820T>A	ENSP00000507786.1:p.Val607Asp
ENST00000683039.1:c.1820T>A	ENSP00000508303.1:p.Val607Asp
ENST00000683235.1:c.1820T>A	ENSP00000507646.1:p.Val607Asp
ENST00000683381.1:c.1820T>A	ENSP00000508184.1:p.Val607Asp
ENST00000684471.1:n.293T>A
ENST00000684584.1:c.1313T>A	ENSP00000508044.1:p.Val438Asp
ENST00000259008.7:c.1820T>A MANE Select	ENSP00000259008.2:p.Val607Asp
ENST00000259008.6:c.1820T>A	ENSP00000259008.2:p.Val607Asp
ENST00000577598.5:c.1820T>A	ENSP00000464654.1:p.Val607Asp
ENST00000579028.1:c.513T>A
NM_032043.2:c.1820T>A , LRG_300t1:c.1820T>A	NP_114432.2:p.Val607Asp
XM_011525332.1:c.1820T>A	XP_011523634.1:p.Val607Asp
XM_011525333.1:c.1820T>A	XP_011523635.1:p.Val607Asp
XM_011525334.1:c.1820T>A	XP_011523636.1:p.Val607Asp
XM_011525335.1:c.1820T>A	XP_011523637.1:p.Val607Asp
XM_011525336.1:c.1820T>A	XP_011523638.1:p.Val607Asp
XM_011525337.1:c.1794+464T>A	XP_011523639.1:n.1794+464T>A
XM_011525338.1:c.1337T>A	XP_011523640.1:p.Val446Asp
XM_011525339.1:c.1820T>A	XP_011523641.1:p.Val607Asp
XM_011525340.1:c.1820T>A	XP_011523642.1:p.Val607Asp
XM_011525341.1:c.1820T>A	XP_011523643.1:p.Val607Asp
XM_011525332.3:c.1820T>A	XP_011523634.1:p.Val607Asp
XM_011525333.3:c.1820T>A	XP_011523635.1:p.Val607Asp
XM_011525334.2:c.1820T>A	XP_011523636.1:p.Val607Asp
XM_011525335.3:c.1820T>A	XP_011523637.1:p.Val607Asp
XM_011525336.2:c.1820T>A	XP_011523638.1:p.Val607Asp
XM_011525337.2:c.1794+464T>A	XP_011523639.1:n.1794+464T>A
XM_011525338.2:c.1337T>A	XP_011523640.1:p.Val446Asp
XM_011525339.3:c.1820T>A	XP_011523641.1:p.Val607Asp
XM_011525340.3:c.1820T>A	XP_011523642.1:p.Val607Asp
XM_011525341.3:c.1820T>A	XP_011523643.1:p.Val607Asp
XM_017025200.1:c.1337T>A	XP_016880689.1:p.Val446Asp
XM_017025201.1:c.1277T>A	XP_016880690.1:p.Val426Asp
NM_032043.3:c.1820T>A MANE Select	NP_114432.2:p.Val607Asp