Canonical Allele Identifier: CA2269199734
Gene: BRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61850081_61850094delinsATTTAACAATCTTT , CM000679.2:g.61850081_61850094delinsATTTAACAATCTTT GRCh38
NC_000017.10:g.59927442_59927455delinsATTTAACAATCTTT , CM000679.1:g.59927442_59927455delinsATTTAACAATCTTT GRCh37
NC_000017.9:g.57282224_57282237delinsATTTAACAATCTTT NCBI36
NG_007409.2:g.18466_18479delinsAAAGATTGTTAAAT , LRG_300:g.18466_18479delinsAAAGATTGTTAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000577913.2:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000462274.2:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000584322.2:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000463272.2:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000682369.1:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000507450.1:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000682453.1:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000506943.1:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000682477.1:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000507075.1:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000682589.1:n.2121-838_2121-825delinsAAAGATTGTTAAAT
ENST00000682755.1:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000507660.1:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000682989.1:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000507786.1:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000683039.1:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000508303.1:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000683235.1:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000507646.1:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000683381.1:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000508184.1:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000683672.1:c.83-2874_83-2861delinsAAAGATTGTTAAAT ENSP00000506781.1:n.83-2874_83-2861delinsAAAGATTGTTAAAT
ENST00000259008.7:c.380-838_380-825delinsAAAGATTGTTAAAT MANE Select ENSP00000259008.2:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000259008.6:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000259008.2:n.380-838_380-825delinsAAAGATTGTTAAAT
ENST00000577598.5:c.380-838_380-825delinsAAAGATTGTTAAAT ENSP00000464654.1:n.380-838_380-825delinsAAAGATTGTTAAAT
NM_032043.2:c.380-838_380-825delinsAAAGATTGTTAAAT , LRG_300t1:c.380-838_380-825delinsAAAGATTGTTAAAT NP_114432.2:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525332.1:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523634.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525333.1:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523635.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525334.1:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523636.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525335.1:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523637.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525336.1:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523638.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525337.1:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523639.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525338.1:c.25-2874_25-2861delinsAAAGATTGTTAAAT XP_011523640.1:n.25-2874_25-2861delinsAAAGATTGTTAAAT
XM_011525339.1:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523641.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525340.1:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523642.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525341.1:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523643.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525332.3:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523634.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525333.3:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523635.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525334.2:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523636.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525335.3:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523637.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525336.2:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523638.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525337.2:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523639.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525338.2:c.25-2874_25-2861delinsAAAGATTGTTAAAT XP_011523640.1:n.25-2874_25-2861delinsAAAGATTGTTAAAT
XM_011525339.3:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523641.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525340.3:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523642.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_011525341.3:c.380-838_380-825delinsAAAGATTGTTAAAT XP_011523643.1:n.380-838_380-825delinsAAAGATTGTTAAAT
XM_017025200.1:c.25-2874_25-2861delinsAAAGATTGTTAAAT XP_016880689.1:n.25-2874_25-2861delinsAAAGATTGTTAAAT
NM_032043.3:c.380-838_380-825delinsAAAGATTGTTAAAT MANE Select NP_114432.2:n.380-838_380-825delinsAAAGATTGTTAAAT