Canonical Allele Identifier: CA400479629

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144087136
• MyVariant Identifiers: chr17:g.59761278A>T (hg19) ; chr17:g.61683917A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683917A>T , CM000679.2:g.61683917A>T	GRCh38
NC_000017.10:g.59761278A>T , CM000679.1:g.59761278A>T	GRCh37
NC_000017.9:g.57116060A>T	NCBI36
NG_007409.2:g.184643T>A , LRG_300:g.184643T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1869T>A
ENST00000682453.1:c.3129T>A	ENSP00000506943.1:p.Ser1043Arg
ENST00000682477.1:c.*2555T>A	ENSP00000507075.1:n.*2555T>A
ENST00000682589.1:n.9006T>A
ENST00000682755.1:c.2907T>A	ENSP00000507660.1:p.Ser969Arg
ENST00000682989.1:c.*220T>A	ENSP00000507786.1:n.*220T>A
ENST00000683039.1:c.3129T>A	ENSP00000508303.1:p.Ser1043Arg
ENST00000683235.1:c.*544T>A	ENSP00000507646.1:n.*544T>A
ENST00000683535.1:n.1259T>A
ENST00000684584.1:c.2292T>A	ENSP00000508044.1:p.Ser764Arg
ENST00000684626.1:n.1375T>A
ENST00000684769.1:c.1319T>A	ENSP00000507691.1:n.1319T>A
ENST00000259008.7:c.3129T>A MANE Select	ENSP00000259008.2:p.Ser1043Arg
ENST00000259008.6:c.3129T>A	ENSP00000259008.2:p.Ser1043Arg
NM_032043.2:c.3129T>A , LRG_300t1:c.3129T>A	NP_114432.2:p.Ser1043Arg
XM_011525332.1:c.3189T>A	XP_011523634.1:p.Ser1063Arg
XM_011525333.1:c.3189T>A	XP_011523635.1:p.Ser1063Arg
XM_011525334.1:c.3189T>A	XP_011523636.1:p.Ser1063Arg
XM_011525335.1:c.3129T>A	XP_011523637.1:p.Ser1043Arg
XM_011525336.1:c.3069T>A	XP_011523638.1:p.Ser1023Arg
XM_011525337.1:c.2988T>A	XP_011523639.1:p.Ser996Arg
XM_011525338.1:c.2706T>A	XP_011523640.1:p.Ser902Arg
XM_011525332.3:c.3189T>A	XP_011523634.1:p.Ser1063Arg
XM_011525333.3:c.3189T>A	XP_011523635.1:p.Ser1063Arg
XM_011525334.2:c.3189T>A	XP_011523636.1:p.Ser1063Arg
XM_011525335.3:c.3129T>A	XP_011523637.1:p.Ser1043Arg
XM_011525336.2:c.3069T>A	XP_011523638.1:p.Ser1023Arg
XM_011525337.2:c.2988T>A	XP_011523639.1:p.Ser996Arg
XM_011525338.2:c.2706T>A	XP_011523640.1:p.Ser902Arg
XM_017025200.1:c.2646T>A	XP_016880689.1:p.Ser882Arg
XM_017025201.1:c.2646T>A	XP_016880690.1:p.Ser882Arg
XM_017025202.1:c.1275T>A	XP_016880691.1:p.Ser425Arg
XM_017025203.1:c.1275T>A	XP_016880692.1:p.Ser425Arg
NM_032043.3:c.3129T>A MANE Select	NP_114432.2:p.Ser1043Arg