Canonical Allele Identifier: CA985272326
Gene: BRIP1 HGNC NCBI

Linked Data

gnomAD v3: 17-61758503-T-TGGGGGGGGGGGG
gnomAD v4: 17-61758503-T-TGGGGGGGGGGGG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61758503_61758504insGGGGGGGGGGGG , CM000679.2:g.61758503_61758504insGGGGGGGGGGGG GRCh38
NC_000017.10:g.59835864_59835865insGGGGGGGGGGGG , CM000679.1:g.59835864_59835865insGGGGGGGGGGGG GRCh37
NC_000017.9:g.57190646_57190647insGGGGGGGGGGGG NCBI36
NG_007409.2:g.110056_110057insCCCCCCCCCCCC , LRG_300:g.110056_110057insCCCCCCCCCCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000579028.2:c.1680-13913_1680-13912insCCCCCCCCCCCC ENSP00000463827.2:n.1680-13913_1680-13912insCCCCCCCCCCCC
ENST00000584322.2:c.2098-13913_2098-13912insCCCCCCCCCCCC ENSP00000463272.2:n.2098-13913_2098-13912insCCCCCCCCCCCC
ENST00000682066.1:c.2227+170_2227+171insCCCCCCCCCCCC ENSP00000507191.1:n.2227+170_2227+171insCCCCCCCCCCCC
ENST00000682073.1:n.838-13913_838-13912insCCCCCCCCCCCC
ENST00000682433.1:n.1177-13913_1177-13912insCCCCCCCCCCCC
ENST00000682453.1:c.2098-13913_2098-13912insCCCCCCCCCCCC ENSP00000506943.1:n.2098-13913_2098-13912insCCCCCCCCCCCC
ENST00000682477.1:c.*1524-13913_*1524-13912insCCCCCCCCCCCC ENSP00000507075.1:n.*1524-13913_*1524-13912insCCCCCCCCCCCC
ENST00000682589.1:n.7975-13913_7975-13912insCCCCCCCCCCCC
ENST00000682755.1:c.1876-13913_1876-13912insCCCCCCCCCCCC ENSP00000507660.1:n.1876-13913_1876-13912insCCCCCCCCCCCC
ENST00000682989.1:c.2098-13913_2098-13912insCCCCCCCCCCCC ENSP00000507786.1:n.2098-13913_2098-13912insCCCCCCCCCCCC
ENST00000683039.1:c.2098-13913_2098-13912insCCCCCCCCCCCC ENSP00000508303.1:n.2098-13913_2098-13912insCCCCCCCCCCCC
ENST00000683235.1:c.2098-13913_2098-13912insCCCCCCCCCCCC ENSP00000507646.1:n.2098-13913_2098-13912insCCCCCCCCCCCC
ENST00000683381.1:c.2158-13913_2158-13912insCCCCCCCCCCCC ENSP00000508184.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
ENST00000683535.1:n.228-13913_228-13912insCCCCCCCCCCCC
ENST00000684471.1:n.511-13913_511-13912insCCCCCCCCCCCC
ENST00000684584.1:c.1591-13913_1591-13912insCCCCCCCCCCCC ENSP00000508044.1:n.1591-13913_1591-13912insCCCCCCCCCCCC
ENST00000684769.1:c.163-13913_163-13912insCCCCCCCCCCCC ENSP00000507691.1:n.163-13913_163-13912insCCCCCCCCCCCC
ENST00000259008.7:c.2098-13913_2098-13912insCCCCCCCCCCCC MANE Select ENSP00000259008.2:n.2098-13913_2098-13912insCCCCCCCCCCCC
ENST00000259008.6:c.2098-13913_2098-13912insCCCCCCCCCCCC ENSP00000259008.2:n.2098-13913_2098-13912insCCCCCCCCCCCC
ENST00000577598.5:c.2098-13913_2098-13912insCCCCCCCCCCCC ENSP00000464654.1:n.2098-13913_2098-13912insCCCCCCCCCCCC
ENST00000584322.1:c.81-13913_81-13912insCCCCCCCCCCCC
NM_032043.2:c.2098-13913_2098-13912insCCCCCCCCCCCC , LRG_300t1:c.2098-13913_2098-13912insCCCCCCCCCCCC NP_114432.2:n.2098-13913_2098-13912insCCCCCCCCCCCC
XM_011525332.1:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523634.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_011525333.1:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523635.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_011525334.1:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523636.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_011525335.1:c.2098-13913_2098-13912insCCCCCCCCCCCC XP_011523637.1:n.2098-13913_2098-13912insCCCCCCCCCCCC
XM_011525336.1:c.2038-13913_2038-13912insCCCCCCCCCCCC XP_011523638.1:n.2038-13913_2038-13912insCCCCCCCCCCCC
XM_011525337.1:c.1957-13913_1957-13912insCCCCCCCCCCCC XP_011523639.1:n.1957-13913_1957-13912insCCCCCCCCCCCC
XM_011525338.1:c.1675-13913_1675-13912insCCCCCCCCCCCC XP_011523640.1:n.1675-13913_1675-13912insCCCCCCCCCCCC
XM_011525339.1:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523641.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_011525340.1:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523642.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_011525332.3:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523634.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_011525333.3:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523635.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_011525334.2:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523636.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_011525335.3:c.2098-13913_2098-13912insCCCCCCCCCCCC XP_011523637.1:n.2098-13913_2098-13912insCCCCCCCCCCCC
XM_011525336.2:c.2038-13913_2038-13912insCCCCCCCCCCCC XP_011523638.1:n.2038-13913_2038-13912insCCCCCCCCCCCC
XM_011525337.2:c.1957-13913_1957-13912insCCCCCCCCCCCC XP_011523639.1:n.1957-13913_1957-13912insCCCCCCCCCCCC
XM_011525338.2:c.1675-13913_1675-13912insCCCCCCCCCCCC XP_011523640.1:n.1675-13913_1675-13912insCCCCCCCCCCCC
XM_011525339.3:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523641.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_011525340.3:c.2158-13913_2158-13912insCCCCCCCCCCCC XP_011523642.1:n.2158-13913_2158-13912insCCCCCCCCCCCC
XM_017025200.1:c.1615-13913_1615-13912insCCCCCCCCCCCC XP_016880689.1:n.1615-13913_1615-13912insCCCCCCCCCCCC
XM_017025201.1:c.1615-13913_1615-13912insCCCCCCCCCCCC XP_016880690.1:n.1615-13913_1615-13912insCCCCCCCCCCCC
XM_017025202.1:c.244-13913_244-13912insCCCCCCCCCCCC XP_016880691.1:n.244-13913_244-13912insCCCCCCCCCCCC
XM_017025203.1:c.244-13913_244-13912insCCCCCCCCCCCC XP_016880692.1:n.244-13913_244-13912insCCCCCCCCCCCC
NM_032043.3:c.2098-13913_2098-13912insCCCCCCCCCCCC MANE Select NP_114432.2:n.2098-13913_2098-13912insCCCCCCCCCCCC
Search 100 bp 5'
Search 100 bp 3'