Canonical Allele Identifier: CA400481349

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144109157
• MyVariant Identifiers: chr17:g.59763257G>T (hg19) ; chr17:g.61685896G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61685896G>T , CM000679.2:g.61685896G>T	GRCh38
NC_000017.10:g.59763257G>T , CM000679.1:g.59763257G>T	GRCh37
NC_000017.9:g.57118039G>T	NCBI36
NG_007409.2:g.182664C>A , LRG_300:g.182664C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682066.1:c.2975C>A	ENSP00000507191.1:n.2975C>A
ENST00000682073.1:n.1585C>A
ENST00000682433.1:n.1924C>A
ENST00000682453.1:c.2845C>A	ENSP00000506943.1:p.Pro949Thr
ENST00000682477.1:c.*2271C>A	ENSP00000507075.1:n.*2271C>A
ENST00000682589.1:n.8722C>A
ENST00000682755.1:c.2623C>A	ENSP00000507660.1:p.Pro875Thr
ENST00000682989.1:c.2610-1756C>A	ENSP00000507786.1:n.2610-1756C>A
ENST00000683039.1:c.2845C>A	ENSP00000508303.1:p.Pro949Thr
ENST00000683235.1:c.*260C>A	ENSP00000507646.1:n.*260C>A
ENST00000683535.1:n.975C>A
ENST00000684471.1:n.1258C>A
ENST00000684584.1:c.2069-1756C>A	ENSP00000508044.1:n.2069-1756C>A
ENST00000684626.1:n.1091C>A
ENST00000684769.1:c.1035C>A	ENSP00000507691.1:n.1035C>A
ENST00000259008.7:c.2845C>A MANE Select	ENSP00000259008.2:p.Pro949Thr
ENST00000259008.6:c.2845C>A	ENSP00000259008.2:p.Pro949Thr
ENST00000577598.5:c.2845C>A	ENSP00000464654.1:p.Pro949Thr
NM_032043.2:c.2845C>A , LRG_300t1:c.2845C>A	NP_114432.2:p.Pro949Thr
XM_011525332.1:c.2905C>A	XP_011523634.1:p.Pro969Thr
XM_011525333.1:c.2905C>A	XP_011523635.1:p.Pro969Thr
XM_011525334.1:c.2905C>A	XP_011523636.1:p.Pro969Thr
XM_011525335.1:c.2845C>A	XP_011523637.1:p.Pro949Thr
XM_011525336.1:c.2785C>A	XP_011523638.1:p.Pro929Thr
XM_011525337.1:c.2704C>A	XP_011523639.1:p.Pro902Thr
XM_011525338.1:c.2422C>A	XP_011523640.1:p.Pro808Thr
XM_011525332.3:c.2905C>A	XP_011523634.1:p.Pro969Thr
XM_011525333.3:c.2905C>A	XP_011523635.1:p.Pro969Thr
XM_011525334.2:c.2905C>A	XP_011523636.1:p.Pro969Thr
XM_011525335.3:c.2845C>A	XP_011523637.1:p.Pro949Thr
XM_011525336.2:c.2785C>A	XP_011523638.1:p.Pro929Thr
XM_011525337.2:c.2704C>A	XP_011523639.1:p.Pro902Thr
XM_011525338.2:c.2422C>A	XP_011523640.1:p.Pro808Thr
XM_017025200.1:c.2362C>A	XP_016880689.1:p.Pro788Thr
XM_017025201.1:c.2362C>A	XP_016880690.1:p.Pro788Thr
XM_017025202.1:c.991C>A	XP_016880691.1:p.Pro331Thr
XM_017025203.1:c.991C>A	XP_016880692.1:p.Pro331Thr
NM_032043.3:c.2845C>A MANE Select	NP_114432.2:p.Pro949Thr