Canonical Allele Identifier: CA400478922

Gene: BRIP1

Linked Data

• dbSNP Id: rs1555572672
• COSMIC: COSM291253
• MyVariant Identifiers: chr17:g.59761057G>C (hg19) ; chr17:g.61683696G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683696G>C , CM000679.2:g.61683696G>C	GRCh38
NC_000017.10:g.59761057G>C , CM000679.1:g.59761057G>C	GRCh37
NC_000017.9:g.57115839G>C	NCBI36
NG_007409.2:g.184864C>G , LRG_300:g.184864C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2090C>G
ENST00000682453.1:c.3350C>G	ENSP00000506943.1:p.Ser1117Ter
ENST00000682477.1:c.*2776C>G	ENSP00000507075.1:n.*2776C>G
ENST00000682589.1:n.9227C>G
ENST00000682755.1:c.3128C>G	ENSP00000507660.1:p.Ser1043Ter
ENST00000682989.1:c.*441C>G	ENSP00000507786.1:n.*441C>G
ENST00000683039.1:c.3350C>G	ENSP00000508303.1:p.Ser1117Ter
ENST00000683235.1:c.*765C>G	ENSP00000507646.1:n.*765C>G
ENST00000683535.1:n.1480C>G
ENST00000684584.1:c.2513C>G	ENSP00000508044.1:p.Ser838Ter
ENST00000684626.1:n.1596C>G
ENST00000684769.1:c.1540C>G	ENSP00000507691.1:n.1540C>G
ENST00000259008.7:c.3350C>G MANE Select	ENSP00000259008.2:p.Ser1117Ter
ENST00000259008.6:c.3350C>G	ENSP00000259008.2:p.Ser1117Ter
NM_032043.2:c.3350C>G , LRG_300t1:c.3350C>G	NP_114432.2:p.Ser1117Ter
XM_011525332.1:c.3410C>G	XP_011523634.1:p.Ser1137Ter
XM_011525333.1:c.3410C>G	XP_011523635.1:p.Ser1137Ter
XM_011525334.1:c.3410C>G	XP_011523636.1:p.Ser1137Ter
XM_011525335.1:c.3350C>G	XP_011523637.1:p.Ser1117Ter
XM_011525336.1:c.3290C>G	XP_011523638.1:p.Ser1097Ter
XM_011525337.1:c.3209C>G	XP_011523639.1:p.Ser1070Ter
XM_011525338.1:c.2927C>G	XP_011523640.1:p.Ser976Ter
XM_011525332.3:c.3410C>G	XP_011523634.1:p.Ser1137Ter
XM_011525333.3:c.3410C>G	XP_011523635.1:p.Ser1137Ter
XM_011525334.2:c.3410C>G	XP_011523636.1:p.Ser1137Ter
XM_011525335.3:c.3350C>G	XP_011523637.1:p.Ser1117Ter
XM_011525336.2:c.3290C>G	XP_011523638.1:p.Ser1097Ter
XM_011525337.2:c.3209C>G	XP_011523639.1:p.Ser1070Ter
XM_011525338.2:c.2927C>G	XP_011523640.1:p.Ser976Ter
XM_017025200.1:c.2867C>G	XP_016880689.1:p.Ser956Ter
XM_017025201.1:c.2867C>G	XP_016880690.1:p.Ser956Ter
XM_017025202.1:c.1496C>G	XP_016880691.1:p.Ser499Ter
XM_017025203.1:c.1496C>G	XP_016880692.1:p.Ser499Ter
NM_032043.3:c.3350C>G MANE Select	NP_114432.2:p.Ser1117Ter