Canonical Allele Identifier: CA16620547
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421072
ClinVar RCV Id: RCV000484917 RCV000804981 RCV002455925
dbSNP Id: rs1064794890
MyVariant Identifiers: chr17:g.59934555del (hg19) chr17:g.61857194del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61857195del , CM000679.2:g.61857195del GRCh38
NC_000017.10:g.59934556del , CM000679.1:g.59934556del GRCh37
NC_000017.9:g.57289338del NCBI36
NG_007409.2:g.11366del , LRG_300:g.11366del

Transcript Alleles

HGVS Amino-acid change
ENST00000577913.2:c.243del ENSP00000462274.2:p.Val82TyrfsTer19
ENST00000584322.2:c.243del ENSP00000463272.2:p.Val82TyrfsTer19
ENST00000682369.1:c.243del ENSP00000507450.1:p.Val82TyrfsTer19
ENST00000682453.1:c.243del ENSP00000506943.1:p.Val82TyrfsTer19
ENST00000682477.1:c.243del ENSP00000507075.1:p.Val82TyrfsTer19
ENST00000682589.1:n.1984del
ENST00000682755.1:c.243del ENSP00000507660.1:p.Val82TyrfsTer19
ENST00000682989.1:c.243del ENSP00000507786.1:p.Val82TyrfsTer19
ENST00000683039.1:c.243del ENSP00000508303.1:p.Val82TyrfsTer19
ENST00000683235.1:c.243del ENSP00000507646.1:p.Val82TyrfsTer19
ENST00000683381.1:c.243del ENSP00000508184.1:p.Val82TyrfsTer19
ENST00000683672.1:c.-55del ENSP00000506781.1:n.-55del
ENST00000259008.7:c.243del MANE Select ENSP00000259008.2:p.Val82TyrfsTer19
ENST00000259008.6:c.243del ENSP00000259008.2:p.Val82TyrfsTer19
ENST00000577598.5:c.243del ENSP00000464654.1:p.Val82TyrfsTer19
NM_032043.2:c.243del , LRG_300t1:c.243del NP_114432.2:p.Val82TyrfsTer19
XM_011525332.1:c.243del XP_011523634.1:p.Val82TyrfsTer19
XM_011525333.1:c.243del XP_011523635.1:p.Val82TyrfsTer19
XM_011525334.1:c.243del XP_011523636.1:p.Val82TyrfsTer19
XM_011525335.1:c.243del XP_011523637.1:p.Val82TyrfsTer19
XM_011525336.1:c.243del XP_011523638.1:p.Val82TyrfsTer19
XM_011525337.1:c.243del XP_011523639.1:p.Val82TyrfsTer19
XM_011525339.1:c.243del XP_011523641.1:p.Val82TyrfsTer19
XM_011525340.1:c.243del XP_011523642.1:p.Val82TyrfsTer19
XM_011525341.1:c.243del XP_011523643.1:p.Val82TyrfsTer19
XM_011525332.3:c.243del XP_011523634.1:p.Val82TyrfsTer19
XM_011525333.3:c.243del XP_011523635.1:p.Val82TyrfsTer19
XM_011525334.2:c.243del XP_011523636.1:p.Val82TyrfsTer19
XM_011525335.3:c.243del XP_011523637.1:p.Val82TyrfsTer19
XM_011525336.2:c.243del XP_011523638.1:p.Val82TyrfsTer19
XM_011525337.2:c.243del XP_011523639.1:p.Val82TyrfsTer19
XM_011525339.3:c.243del XP_011523641.1:p.Val82TyrfsTer19
XM_011525340.3:c.243del XP_011523642.1:p.Val82TyrfsTer19
XM_011525341.3:c.243del XP_011523643.1:p.Val82TyrfsTer19
NM_032043.3:c.243del MANE Select NP_114432.2:p.Val82TyrfsTer19
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