Canonical Allele Identifier: CA400478585
Gene: BRIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61683562A>G , CM000679.2:g.61683562A>G GRCh38
NC_000017.10:g.59760923A>G , CM000679.1:g.59760923A>G GRCh37
NC_000017.9:g.57115705A>G NCBI36
NG_007409.2:g.184998T>C , LRG_300:g.184998T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682073.1:n.2224T>C
ENST00000682453.1:c.3484T>C ENSP00000506943.1:p.Ser1162Pro
ENST00000682477.1:c.*2910T>C ENSP00000507075.1:n.*2910T>C
ENST00000682589.1:n.9361T>C
ENST00000682755.1:c.3262T>C ENSP00000507660.1:p.Ser1088Pro
ENST00000682989.1:c.*575T>C ENSP00000507786.1:n.*575T>C
ENST00000683039.1:c.3484T>C ENSP00000508303.1:p.Ser1162Pro
ENST00000683235.1:c.*899T>C ENSP00000507646.1:n.*899T>C
ENST00000683535.1:n.1614T>C
ENST00000684584.1:c.2647T>C ENSP00000508044.1:p.Ser883Pro
ENST00000684626.1:n.1730T>C
ENST00000684769.1:c.1674T>C ENSP00000507691.1:n.1674T>C
ENST00000259008.7:c.3484T>C MANE Select ENSP00000259008.2:p.Ser1162Pro
ENST00000259008.6:c.3484T>C ENSP00000259008.2:p.Ser1162Pro
NM_032043.2:c.3484T>C , LRG_300t1:c.3484T>C NP_114432.2:p.Ser1162Pro
XM_011525332.1:c.3544T>C XP_011523634.1:p.Ser1182Pro
XM_011525333.1:c.3544T>C XP_011523635.1:p.Ser1182Pro
XM_011525334.1:c.3544T>C XP_011523636.1:p.Ser1182Pro
XM_011525335.1:c.3484T>C XP_011523637.1:p.Ser1162Pro
XM_011525336.1:c.3424T>C XP_011523638.1:p.Ser1142Pro
XM_011525337.1:c.3343T>C XP_011523639.1:p.Ser1115Pro
XM_011525338.1:c.3061T>C XP_011523640.1:p.Ser1021Pro
XM_011525332.3:c.3544T>C XP_011523634.1:p.Ser1182Pro
XM_011525333.3:c.3544T>C XP_011523635.1:p.Ser1182Pro
XM_011525334.2:c.3544T>C XP_011523636.1:p.Ser1182Pro
XM_011525335.3:c.3484T>C XP_011523637.1:p.Ser1162Pro
XM_011525336.2:c.3424T>C XP_011523638.1:p.Ser1142Pro
XM_011525337.2:c.3343T>C XP_011523639.1:p.Ser1115Pro
XM_011525338.2:c.3061T>C XP_011523640.1:p.Ser1021Pro
XM_017025200.1:c.3001T>C XP_016880689.1:p.Ser1001Pro
XM_017025201.1:c.3001T>C XP_016880690.1:p.Ser1001Pro
XM_017025202.1:c.1630T>C XP_016880691.1:p.Ser544Pro
XM_017025203.1:c.1630T>C XP_016880692.1:p.Ser544Pro
NM_032043.3:c.3484T>C MANE Select NP_114432.2:p.Ser1162Pro