Canonical Allele Identifier: CA2269131869
Gene: BRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61685908C= , CM000679.2:g.61685908C= GRCh38
NC_000017.10:g.59763269C= , CM000679.1:g.59763269C= GRCh37
NC_000017.9:g.57118051C= NCBI36
NG_007409.2:g.182652G= , LRG_300:g.182652G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682066.1:c.2963G= ENSP00000507191.1:n.2963G=
ENST00000682073.1:n.1573G=
ENST00000682433.1:n.1912G=
ENST00000682453.1:c.2833G= ENSP00000506943.1:p.Glu945=
ENST00000682477.1:c.*2259G= ENSP00000507075.1:n.*2259G=
ENST00000682589.1:n.8710G=
ENST00000682755.1:c.2611G= ENSP00000507660.1:p.Glu871=
ENST00000682989.1:c.2610-1768G= ENSP00000507786.1:n.2610-1768G=
ENST00000683039.1:c.2833G= ENSP00000508303.1:p.Glu945=
ENST00000683235.1:c.*248G= ENSP00000507646.1:n.*248G=
ENST00000683535.1:n.963G=
ENST00000684471.1:n.1246G=
ENST00000684584.1:c.2069-1768G= ENSP00000508044.1:n.2069-1768G=
ENST00000684626.1:n.1079G=
ENST00000684769.1:c.1023G= ENSP00000507691.1:n.1023G=
ENST00000259008.7:c.2833G= MANE Select ENSP00000259008.2:p.Glu945=
ENST00000259008.6:c.2833G= ENSP00000259008.2:p.Glu945=
ENST00000577598.5:c.2833G= ENSP00000464654.1:p.Glu945=
NM_032043.2:c.2833G= , LRG_300t1:c.2833G= NP_114432.2:p.Glu945=
XM_011525332.1:c.2893G= XP_011523634.1:p.Glu965=
XM_011525333.1:c.2893G= XP_011523635.1:p.Glu965=
XM_011525334.1:c.2893G= XP_011523636.1:p.Glu965=
XM_011525335.1:c.2833G= XP_011523637.1:p.Glu945=
XM_011525336.1:c.2773G= XP_011523638.1:p.Glu925=
XM_011525337.1:c.2692G= XP_011523639.1:p.Glu898=
XM_011525338.1:c.2410G= XP_011523640.1:p.Glu804=
XM_011525332.3:c.2893G= XP_011523634.1:p.Glu965=
XM_011525333.3:c.2893G= XP_011523635.1:p.Glu965=
XM_011525334.2:c.2893G= XP_011523636.1:p.Glu965=
XM_011525335.3:c.2833G= XP_011523637.1:p.Glu945=
XM_011525336.2:c.2773G= XP_011523638.1:p.Glu925=
XM_011525337.2:c.2692G= XP_011523639.1:p.Glu898=
XM_011525338.2:c.2410G= XP_011523640.1:p.Glu804=
XM_017025200.1:c.2350G= XP_016880689.1:p.Glu784=
XM_017025201.1:c.2350G= XP_016880690.1:p.Glu784=
XM_017025202.1:c.979G= XP_016880691.1:p.Glu327=
XM_017025203.1:c.979G= XP_016880692.1:p.Glu327=
NM_032043.3:c.2833G= MANE Select NP_114432.2:p.Glu945=