Canonical Allele Identifier: CA891844433
Gene: BRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 565330
ClinVar RCV Id: RCV000684867

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61859815_61862787del , CM000679.2:g.61859815_61862787del GRCh38
NC_000017.10:g.59937176_59940148del , CM000679.1:g.59937176_59940148del GRCh37
NC_000017.9:g.57291958_57294930del NCBI36
NG_007409.2:g.5774_8746del , LRG_300:g.5774_8746del

Transcript Alleles

HGVS Amino-acid change
ENST00000577913.2:c.-27+498_187del
ENST00000584322.2:c.-31+498_187del
ENST00000682369.1:c.-31+498_187del
ENST00000682453.1:c.-31+498_187del
ENST00000682477.1:c.-31+498_187del
ENST00000682589.1:n.495_1928del
ENST00000682989.1:c.-27+498_187del
ENST00000683039.1:c.-197+498_187del
ENST00000683235.1:c.-27+498_187del
ENST00000683381.1:c.-31+498_187del
ENST00000683672.1:c.-93+498_-92-2583del ENSP00000506781.1:n.-93+498_-92-2583del
ENST00000259008.7:c.-31+498_187del
ENST00000259008.6:c.-31+498_187del
ENST00000577913.1:c.-197+498_187del
NM_032043.2:c.-31+498_187del , LRG_300t1:c.-31+498_187del
XM_011525332.1:c.-31+498_187del
XM_011525333.1:c.-27+498_187del
XM_011525335.1:c.-31+498_187del
XM_011525336.1:c.-31+498_187del
XM_011525337.1:c.-31+498_187del
XM_011525339.1:c.-31+498_187del
XM_011525340.1:c.-31+498_187del
XM_011525341.1:c.-31+498_187del
XM_011525332.3:c.-31+498_187del
XM_011525333.3:c.-27+498_187del
XM_011525334.2:c.-907_187del
XM_011525335.3:c.-31+498_187del
XM_011525336.2:c.-31+498_187del
XM_011525337.2:c.-31+498_187del
XM_011525339.3:c.-31+498_187del
XM_011525340.3:c.-31+498_187del
XM_011525341.3:c.-31+498_187del
NM_032043.3:c.-31+498_187del