Canonical Allele Identifier: CA400477921
Gene: BRIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61683405T>A , CM000679.2:g.61683405T>A GRCh38
NC_000017.10:g.59760766T>A , CM000679.1:g.59760766T>A GRCh37
NC_000017.9:g.57115548T>A NCBI36
NG_007409.2:g.185155A>T , LRG_300:g.185155A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682073.1:n.2381A>T
ENST00000682453.1:c.3641A>T ENSP00000506943.1:p.Lys1214Ile
ENST00000682477.1:c.*3067A>T ENSP00000507075.1:n.*3067A>T
ENST00000682589.1:n.9518A>T
ENST00000682755.1:c.3419A>T ENSP00000507660.1:p.Lys1140Ile
ENST00000682989.1:c.*732A>T ENSP00000507786.1:n.*732A>T
ENST00000683039.1:c.3641A>T ENSP00000508303.1:p.Lys1214Ile
ENST00000683235.1:c.*1056A>T ENSP00000507646.1:n.*1056A>T
ENST00000683535.1:n.1771A>T
ENST00000684584.1:c.2804A>T ENSP00000508044.1:p.Lys935Ile
ENST00000684626.1:n.1887A>T
ENST00000684769.1:c.1831A>T ENSP00000507691.1:n.1831A>T
ENST00000259008.7:c.3641A>T MANE Select ENSP00000259008.2:p.Lys1214Ile
ENST00000259008.6:c.3641A>T ENSP00000259008.2:p.Lys1214Ile
NM_032043.2:c.3641A>T , LRG_300t1:c.3641A>T NP_114432.2:p.Lys1214Ile
XM_011525332.1:c.3701A>T XP_011523634.1:p.Lys1234Ile
XM_011525333.1:c.3701A>T XP_011523635.1:p.Lys1234Ile
XM_011525334.1:c.3701A>T XP_011523636.1:p.Lys1234Ile
XM_011525335.1:c.3641A>T XP_011523637.1:p.Lys1214Ile
XM_011525336.1:c.3581A>T XP_011523638.1:p.Lys1194Ile
XM_011525337.1:c.3500A>T XP_011523639.1:p.Lys1167Ile
XM_011525338.1:c.3218A>T XP_011523640.1:p.Lys1073Ile
XM_011525332.3:c.3701A>T XP_011523634.1:p.Lys1234Ile
XM_011525333.3:c.3701A>T XP_011523635.1:p.Lys1234Ile
XM_011525334.2:c.3701A>T XP_011523636.1:p.Lys1234Ile
XM_011525335.3:c.3641A>T XP_011523637.1:p.Lys1214Ile
XM_011525336.2:c.3581A>T XP_011523638.1:p.Lys1194Ile
XM_011525337.2:c.3500A>T XP_011523639.1:p.Lys1167Ile
XM_011525338.2:c.3218A>T XP_011523640.1:p.Lys1073Ile
XM_017025200.1:c.3158A>T XP_016880689.1:p.Lys1053Ile
XM_017025201.1:c.3158A>T XP_016880690.1:p.Lys1053Ile
XM_017025202.1:c.1787A>T XP_016880691.1:p.Lys596Ile
XM_017025203.1:c.1787A>T XP_016880692.1:p.Lys596Ile
NM_032043.3:c.3641A>T MANE Select NP_114432.2:p.Lys1214Ile