Canonical Allele Identifier: CA400478436

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 1496891
• ClinVar RCV Id: RCV001992111
• dbSNP Id: rs2144073209
• MyVariant Identifiers: chr17:g.59760887T>C (hg19) ; chr17:g.61683526T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683526T>C , CM000679.2:g.61683526T>C	GRCh38
NC_000017.10:g.59760887T>C , CM000679.1:g.59760887T>C	GRCh37
NC_000017.9:g.57115669T>C	NCBI36
NG_007409.2:g.185034A>G , LRG_300:g.185034A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2260A>G
ENST00000682453.1:c.3520A>G	ENSP00000506943.1:p.Arg1174Gly
ENST00000682477.1:c.*2946A>G	ENSP00000507075.1:n.*2946A>G
ENST00000682589.1:n.9397A>G
ENST00000682755.1:c.3298A>G	ENSP00000507660.1:p.Arg1100Gly
ENST00000682989.1:c.*611A>G	ENSP00000507786.1:n.*611A>G
ENST00000683039.1:c.3520A>G	ENSP00000508303.1:p.Arg1174Gly
ENST00000683235.1:c.*935A>G	ENSP00000507646.1:n.*935A>G
ENST00000683535.1:n.1650A>G
ENST00000684584.1:c.2683A>G	ENSP00000508044.1:p.Arg895Gly
ENST00000684626.1:n.1766A>G
ENST00000684769.1:c.1710A>G	ENSP00000507691.1:n.1710A>G
ENST00000259008.7:c.3520A>G MANE Select	ENSP00000259008.2:p.Arg1174Gly
ENST00000259008.6:c.3520A>G	ENSP00000259008.2:p.Arg1174Gly
NM_032043.2:c.3520A>G , LRG_300t1:c.3520A>G	NP_114432.2:p.Arg1174Gly
XM_011525332.1:c.3580A>G	XP_011523634.1:p.Arg1194Gly
XM_011525333.1:c.3580A>G	XP_011523635.1:p.Arg1194Gly
XM_011525334.1:c.3580A>G	XP_011523636.1:p.Arg1194Gly
XM_011525335.1:c.3520A>G	XP_011523637.1:p.Arg1174Gly
XM_011525336.1:c.3460A>G	XP_011523638.1:p.Arg1154Gly
XM_011525337.1:c.3379A>G	XP_011523639.1:p.Arg1127Gly
XM_011525338.1:c.3097A>G	XP_011523640.1:p.Arg1033Gly
XM_011525332.3:c.3580A>G	XP_011523634.1:p.Arg1194Gly
XM_011525333.3:c.3580A>G	XP_011523635.1:p.Arg1194Gly
XM_011525334.2:c.3580A>G	XP_011523636.1:p.Arg1194Gly
XM_011525335.3:c.3520A>G	XP_011523637.1:p.Arg1174Gly
XM_011525336.2:c.3460A>G	XP_011523638.1:p.Arg1154Gly
XM_011525337.2:c.3379A>G	XP_011523639.1:p.Arg1127Gly
XM_011525338.2:c.3097A>G	XP_011523640.1:p.Arg1033Gly
XM_017025200.1:c.3037A>G	XP_016880689.1:p.Arg1013Gly
XM_017025201.1:c.3037A>G	XP_016880690.1:p.Arg1013Gly
XM_017025202.1:c.1666A>G	XP_016880691.1:p.Arg556Gly
XM_017025203.1:c.1666A>G	XP_016880692.1:p.Arg556Gly
NM_032043.3:c.3520A>G MANE Select	NP_114432.2:p.Arg1174Gly