Canonical Allele Identifier: CA400479063

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144081768
• MyVariant Identifiers: chr17:g.59761125A>C (hg19) ; chr17:g.61683764A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683764A>C , CM000679.2:g.61683764A>C	GRCh38
NC_000017.10:g.59761125A>C , CM000679.1:g.59761125A>C	GRCh37
NC_000017.9:g.57115907A>C	NCBI36
NG_007409.2:g.184796T>G , LRG_300:g.184796T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2022T>G
ENST00000682453.1:c.3282T>G	ENSP00000506943.1:p.Cys1094Trp
ENST00000682477.1:c.*2708T>G	ENSP00000507075.1:n.*2708T>G
ENST00000682589.1:n.9159T>G
ENST00000682755.1:c.3060T>G	ENSP00000507660.1:p.Cys1020Trp
ENST00000682989.1:c.*373T>G	ENSP00000507786.1:n.*373T>G
ENST00000683039.1:c.3282T>G	ENSP00000508303.1:p.Cys1094Trp
ENST00000683235.1:c.*697T>G	ENSP00000507646.1:n.*697T>G
ENST00000683535.1:n.1412T>G
ENST00000684584.1:c.2445T>G	ENSP00000508044.1:p.Cys815Trp
ENST00000684626.1:n.1528T>G
ENST00000684769.1:c.1472T>G	ENSP00000507691.1:n.1472T>G
ENST00000259008.7:c.3282T>G MANE Select	ENSP00000259008.2:p.Cys1094Trp
ENST00000259008.6:c.3282T>G	ENSP00000259008.2:p.Cys1094Trp
NM_032043.2:c.3282T>G , LRG_300t1:c.3282T>G	NP_114432.2:p.Cys1094Trp
XM_011525332.1:c.3342T>G	XP_011523634.1:p.Cys1114Trp
XM_011525333.1:c.3342T>G	XP_011523635.1:p.Cys1114Trp
XM_011525334.1:c.3342T>G	XP_011523636.1:p.Cys1114Trp
XM_011525335.1:c.3282T>G	XP_011523637.1:p.Cys1094Trp
XM_011525336.1:c.3222T>G	XP_011523638.1:p.Cys1074Trp
XM_011525337.1:c.3141T>G	XP_011523639.1:p.Cys1047Trp
XM_011525338.1:c.2859T>G	XP_011523640.1:p.Cys953Trp
XM_011525332.3:c.3342T>G	XP_011523634.1:p.Cys1114Trp
XM_011525333.3:c.3342T>G	XP_011523635.1:p.Cys1114Trp
XM_011525334.2:c.3342T>G	XP_011523636.1:p.Cys1114Trp
XM_011525335.3:c.3282T>G	XP_011523637.1:p.Cys1094Trp
XM_011525336.2:c.3222T>G	XP_011523638.1:p.Cys1074Trp
XM_011525337.2:c.3141T>G	XP_011523639.1:p.Cys1047Trp
XM_011525338.2:c.2859T>G	XP_011523640.1:p.Cys953Trp
XM_017025200.1:c.2799T>G	XP_016880689.1:p.Cys933Trp
XM_017025201.1:c.2799T>G	XP_016880690.1:p.Cys933Trp
XM_017025202.1:c.1428T>G	XP_016880691.1:p.Cys476Trp
XM_017025203.1:c.1428T>G	XP_016880692.1:p.Cys476Trp
NM_032043.3:c.3282T>G MANE Select	NP_114432.2:p.Cys1094Trp