Canonical Allele Identifier: CA2269131864
Gene: BRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61685901T= , CM000679.2:g.61685901T= GRCh38
NC_000017.10:g.59763262T= , CM000679.1:g.59763262T= GRCh37
NC_000017.9:g.57118044T= NCBI36
NG_007409.2:g.182659A= , LRG_300:g.182659A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682066.1:c.2970A= ENSP00000507191.1:n.2970A=
ENST00000682073.1:n.1580A=
ENST00000682433.1:n.1919A=
ENST00000682453.1:c.2840A= ENSP00000506943.1:p.Gln947=
ENST00000682477.1:c.*2266A= ENSP00000507075.1:n.*2266A=
ENST00000682589.1:n.8717A=
ENST00000682755.1:c.2618A= ENSP00000507660.1:p.Gln873=
ENST00000682989.1:c.2610-1761A= ENSP00000507786.1:n.2610-1761A=
ENST00000683039.1:c.2840A= ENSP00000508303.1:p.Gln947=
ENST00000683235.1:c.*255A= ENSP00000507646.1:n.*255A=
ENST00000683535.1:n.970A=
ENST00000684471.1:n.1253A=
ENST00000684584.1:c.2069-1761A= ENSP00000508044.1:n.2069-1761A=
ENST00000684626.1:n.1086A=
ENST00000684769.1:c.1030A= ENSP00000507691.1:n.1030A=
ENST00000259008.7:c.2840A= MANE Select ENSP00000259008.2:p.Gln947=
ENST00000259008.6:c.2840A= ENSP00000259008.2:p.Gln947=
ENST00000577598.5:c.2840A= ENSP00000464654.1:p.Gln947=
NM_032043.2:c.2840A= , LRG_300t1:c.2840A= NP_114432.2:p.Gln947=
XM_011525332.1:c.2900A= XP_011523634.1:p.Gln967=
XM_011525333.1:c.2900A= XP_011523635.1:p.Gln967=
XM_011525334.1:c.2900A= XP_011523636.1:p.Gln967=
XM_011525335.1:c.2840A= XP_011523637.1:p.Gln947=
XM_011525336.1:c.2780A= XP_011523638.1:p.Gln927=
XM_011525337.1:c.2699A= XP_011523639.1:p.Gln900=
XM_011525338.1:c.2417A= XP_011523640.1:p.Gln806=
XM_011525332.3:c.2900A= XP_011523634.1:p.Gln967=
XM_011525333.3:c.2900A= XP_011523635.1:p.Gln967=
XM_011525334.2:c.2900A= XP_011523636.1:p.Gln967=
XM_011525335.3:c.2840A= XP_011523637.1:p.Gln947=
XM_011525336.2:c.2780A= XP_011523638.1:p.Gln927=
XM_011525337.2:c.2699A= XP_011523639.1:p.Gln900=
XM_011525338.2:c.2417A= XP_011523640.1:p.Gln806=
XM_017025200.1:c.2357A= XP_016880689.1:p.Gln786=
XM_017025201.1:c.2357A= XP_016880690.1:p.Gln786=
XM_017025202.1:c.986A= XP_016880691.1:p.Gln329=
XM_017025203.1:c.986A= XP_016880692.1:p.Gln329=
NM_032043.3:c.2840A= MANE Select NP_114432.2:p.Gln947=