Canonical Allele Identifier: CA400478890
Gene: BRIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61683682C>T , CM000679.2:g.61683682C>T GRCh38
NC_000017.10:g.59761043C>T , CM000679.1:g.59761043C>T GRCh37
NC_000017.9:g.57115825C>T NCBI36
NG_007409.2:g.184878G>A , LRG_300:g.184878G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682073.1:n.2104G>A
ENST00000682453.1:c.3364G>A ENSP00000506943.1:p.Glu1122Lys
ENST00000682477.1:c.*2790G>A ENSP00000507075.1:n.*2790G>A
ENST00000682589.1:n.9241G>A
ENST00000682755.1:c.3142G>A ENSP00000507660.1:p.Glu1048Lys
ENST00000682989.1:c.*455G>A ENSP00000507786.1:n.*455G>A
ENST00000683039.1:c.3364G>A ENSP00000508303.1:p.Glu1122Lys
ENST00000683235.1:c.*779G>A ENSP00000507646.1:n.*779G>A
ENST00000683535.1:n.1494G>A
ENST00000684584.1:c.2527G>A ENSP00000508044.1:p.Glu843Lys
ENST00000684626.1:n.1610G>A
ENST00000684769.1:c.1554G>A ENSP00000507691.1:n.1554G>A
ENST00000259008.7:c.3364G>A MANE Select ENSP00000259008.2:p.Glu1122Lys
ENST00000259008.6:c.3364G>A ENSP00000259008.2:p.Glu1122Lys
NM_032043.2:c.3364G>A , LRG_300t1:c.3364G>A NP_114432.2:p.Glu1122Lys
XM_011525332.1:c.3424G>A XP_011523634.1:p.Glu1142Lys
XM_011525333.1:c.3424G>A XP_011523635.1:p.Glu1142Lys
XM_011525334.1:c.3424G>A XP_011523636.1:p.Glu1142Lys
XM_011525335.1:c.3364G>A XP_011523637.1:p.Glu1122Lys
XM_011525336.1:c.3304G>A XP_011523638.1:p.Glu1102Lys
XM_011525337.1:c.3223G>A XP_011523639.1:p.Glu1075Lys
XM_011525338.1:c.2941G>A XP_011523640.1:p.Glu981Lys
XM_011525332.3:c.3424G>A XP_011523634.1:p.Glu1142Lys
XM_011525333.3:c.3424G>A XP_011523635.1:p.Glu1142Lys
XM_011525334.2:c.3424G>A XP_011523636.1:p.Glu1142Lys
XM_011525335.3:c.3364G>A XP_011523637.1:p.Glu1122Lys
XM_011525336.2:c.3304G>A XP_011523638.1:p.Glu1102Lys
XM_011525337.2:c.3223G>A XP_011523639.1:p.Glu1075Lys
XM_011525338.2:c.2941G>A XP_011523640.1:p.Glu981Lys
XM_017025200.1:c.2881G>A XP_016880689.1:p.Glu961Lys
XM_017025201.1:c.2881G>A XP_016880690.1:p.Glu961Lys
XM_017025202.1:c.1510G>A XP_016880691.1:p.Glu504Lys
XM_017025203.1:c.1510G>A XP_016880692.1:p.Glu504Lys
NM_032043.3:c.3364G>A MANE Select NP_114432.2:p.Glu1122Lys