Canonical Allele Identifier: CA196420
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186992
dbSNP Id: rs786203384

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61744581delinsGGA , CM000679.2:g.61744581delinsGGA GRCh38
NC_000017.10:g.59821942delinsGGA , CM000679.1:g.59821942delinsGGA GRCh37
NC_000017.9:g.57176724delinsGGA NCBI36
NG_007409.2:g.123979delinsTCC , LRG_300:g.123979delinsTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000579028.2:c.1690delinsTCC ENSP00000463827.2:n.1690delinsTCC
ENST00000584322.2:c.2108delinsTCC ENSP00000463272.2:p.Lys703IlefsTer3
ENST00000682066.1:c.2238delinsTCC ENSP00000507191.1:n.2238delinsTCC
ENST00000682073.1:n.848delinsTCC
ENST00000682433.1:n.1187delinsTCC
ENST00000682453.1:c.2108delinsTCC ENSP00000506943.1:p.Lys703IlefsTer3
ENST00000682477.1:c.*1534delinsTCC ENSP00000507075.1:n.*1534delinsTCC
ENST00000682589.1:n.7985delinsTCC
ENST00000682755.1:c.1886delinsTCC ENSP00000507660.1:p.Lys629IlefsTer3
ENST00000682989.1:c.2108delinsTCC ENSP00000507786.1:p.Lys703IlefsTer3
ENST00000683039.1:c.2108delinsTCC ENSP00000508303.1:p.Lys703IlefsTer3
ENST00000683235.1:c.2108delinsTCC ENSP00000507646.1:p.Lys703IlefsTer3
ENST00000683381.1:c.2168delinsTCC ENSP00000508184.1:p.Lys723IlefsTer3
ENST00000683535.1:n.238delinsTCC
ENST00000684471.1:n.521delinsTCC
ENST00000684584.1:c.1601delinsTCC ENSP00000508044.1:p.Lys534IlefsTer3
ENST00000684769.1:c.173delinsTCC ENSP00000507691.1:p.Lys58IlefsTer3
ENST00000259008.7:c.2108delinsTCC MANE Select ENSP00000259008.2:p.Lys703IlefsTer3
ENST00000259008.6:c.2108delinsTCC ENSP00000259008.2:p.Lys703IlefsTer3
ENST00000577598.5:c.2108delinsTCC ENSP00000464654.1:p.Lys703IlefsTer3
ENST00000584322.1:c.91delinsTCC
NM_032043.2:c.2108delinsTCC , LRG_300t1:c.2108delinsTCC NP_114432.2:p.Lys703IlefsTer3
XM_011525332.1:c.2168delinsTCC XP_011523634.1:p.Lys723IlefsTer3
XM_011525333.1:c.2168delinsTCC XP_011523635.1:p.Lys723IlefsTer3
XM_011525334.1:c.2168delinsTCC XP_011523636.1:p.Lys723IlefsTer3
XM_011525335.1:c.2108delinsTCC XP_011523637.1:p.Lys703IlefsTer3
XM_011525336.1:c.2048delinsTCC XP_011523638.1:p.Lys683IlefsTer3
XM_011525337.1:c.1967delinsTCC XP_011523639.1:p.Lys656IlefsTer3
XM_011525338.1:c.1685delinsTCC XP_011523640.1:p.Lys562IlefsTer3
XM_011525339.1:c.2168delinsTCC XP_011523641.1:p.Lys723IlefsTer3
XM_011525340.1:c.2168delinsTCC XP_011523642.1:p.Lys723IlefsTer3
XM_011525332.3:c.2168delinsTCC XP_011523634.1:p.Lys723IlefsTer3
XM_011525333.3:c.2168delinsTCC XP_011523635.1:p.Lys723IlefsTer3
XM_011525334.2:c.2168delinsTCC XP_011523636.1:p.Lys723IlefsTer3
XM_011525335.3:c.2108delinsTCC XP_011523637.1:p.Lys703IlefsTer3
XM_011525336.2:c.2048delinsTCC XP_011523638.1:p.Lys683IlefsTer3
XM_011525337.2:c.1967delinsTCC XP_011523639.1:p.Lys656IlefsTer3
XM_011525338.2:c.1685delinsTCC XP_011523640.1:p.Lys562IlefsTer3
XM_011525339.3:c.2168delinsTCC XP_011523641.1:p.Lys723IlefsTer3
XM_011525340.3:c.2168delinsTCC XP_011523642.1:p.Lys723IlefsTer3
XM_017025200.1:c.1625delinsTCC XP_016880689.1:p.Lys542IlefsTer3
XM_017025201.1:c.1625delinsTCC XP_016880690.1:p.Lys542IlefsTer3
XM_017025202.1:c.254delinsTCC XP_016880691.1:p.Lys85IlefsTer3
XM_017025203.1:c.254delinsTCC XP_016880692.1:p.Lys85IlefsTer3
NM_032043.3:c.2108delinsTCC MANE Select NP_114432.2:p.Lys703IlefsTer3