Canonical Allele Identifier: CA400478936

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 568102
• ClinVar RCV Id: RCV000688353
• dbSNP Id: rs1567728281
• MyVariant Identifiers: chr17:g.59761064A>G (hg19) ; chr17:g.61683703A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683703A>G , CM000679.2:g.61683703A>G	GRCh38
NC_000017.10:g.59761064A>G , CM000679.1:g.59761064A>G	GRCh37
NC_000017.9:g.57115846A>G	NCBI36
NG_007409.2:g.184857T>C , LRG_300:g.184857T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2083T>C
ENST00000682453.1:c.3343T>C	ENSP00000506943.1:p.Ser1115Pro
ENST00000682477.1:c.*2769T>C	ENSP00000507075.1:n.*2769T>C
ENST00000682589.1:n.9220T>C
ENST00000682755.1:c.3121T>C	ENSP00000507660.1:p.Ser1041Pro
ENST00000682989.1:c.*434T>C	ENSP00000507786.1:n.*434T>C
ENST00000683039.1:c.3343T>C	ENSP00000508303.1:p.Ser1115Pro
ENST00000683235.1:c.*758T>C	ENSP00000507646.1:n.*758T>C
ENST00000683535.1:n.1473T>C
ENST00000684584.1:c.2506T>C	ENSP00000508044.1:p.Ser836Pro
ENST00000684626.1:n.1589T>C
ENST00000684769.1:c.1533T>C	ENSP00000507691.1:n.1533T>C
ENST00000259008.7:c.3343T>C MANE Select	ENSP00000259008.2:p.Ser1115Pro
ENST00000259008.6:c.3343T>C	ENSP00000259008.2:p.Ser1115Pro
NM_032043.2:c.3343T>C , LRG_300t1:c.3343T>C	NP_114432.2:p.Ser1115Pro
XM_011525332.1:c.3403T>C	XP_011523634.1:p.Ser1135Pro
XM_011525333.1:c.3403T>C	XP_011523635.1:p.Ser1135Pro
XM_011525334.1:c.3403T>C	XP_011523636.1:p.Ser1135Pro
XM_011525335.1:c.3343T>C	XP_011523637.1:p.Ser1115Pro
XM_011525336.1:c.3283T>C	XP_011523638.1:p.Ser1095Pro
XM_011525337.1:c.3202T>C	XP_011523639.1:p.Ser1068Pro
XM_011525338.1:c.2920T>C	XP_011523640.1:p.Ser974Pro
XM_011525332.3:c.3403T>C	XP_011523634.1:p.Ser1135Pro
XM_011525333.3:c.3403T>C	XP_011523635.1:p.Ser1135Pro
XM_011525334.2:c.3403T>C	XP_011523636.1:p.Ser1135Pro
XM_011525335.3:c.3343T>C	XP_011523637.1:p.Ser1115Pro
XM_011525336.2:c.3283T>C	XP_011523638.1:p.Ser1095Pro
XM_011525337.2:c.3202T>C	XP_011523639.1:p.Ser1068Pro
XM_011525338.2:c.2920T>C	XP_011523640.1:p.Ser974Pro
XM_017025200.1:c.2860T>C	XP_016880689.1:p.Ser954Pro
XM_017025201.1:c.2860T>C	XP_016880690.1:p.Ser954Pro
XM_017025202.1:c.1489T>C	XP_016880691.1:p.Ser497Pro
XM_017025203.1:c.1489T>C	XP_016880692.1:p.Ser497Pro
NM_032043.3:c.3343T>C MANE Select	NP_114432.2:p.Ser1115Pro