Canonical Allele Identifier: CA400479263
Gene: BRIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61683826T>G , CM000679.2:g.61683826T>G GRCh38
NC_000017.10:g.59761187T>G , CM000679.1:g.59761187T>G GRCh37
NC_000017.9:g.57115969T>G NCBI36
NG_007409.2:g.184734A>C , LRG_300:g.184734A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682073.1:n.1960A>C
ENST00000682453.1:c.3220A>C ENSP00000506943.1:p.Ile1074Leu
ENST00000682477.1:c.*2646A>C ENSP00000507075.1:n.*2646A>C
ENST00000682589.1:n.9097A>C
ENST00000682755.1:c.2998A>C ENSP00000507660.1:p.Ile1000Leu
ENST00000682989.1:c.*311A>C ENSP00000507786.1:n.*311A>C
ENST00000683039.1:c.3220A>C ENSP00000508303.1:p.Ile1074Leu
ENST00000683235.1:c.*635A>C ENSP00000507646.1:n.*635A>C
ENST00000683535.1:n.1350A>C
ENST00000684584.1:c.2383A>C ENSP00000508044.1:p.Ile795Leu
ENST00000684626.1:n.1466A>C
ENST00000684769.1:c.1410A>C ENSP00000507691.1:n.1410A>C
ENST00000259008.7:c.3220A>C MANE Select ENSP00000259008.2:p.Ile1074Leu
ENST00000259008.6:c.3220A>C ENSP00000259008.2:p.Ile1074Leu
NM_032043.2:c.3220A>C , LRG_300t1:c.3220A>C NP_114432.2:p.Ile1074Leu
XM_011525332.1:c.3280A>C XP_011523634.1:p.Ile1094Leu
XM_011525333.1:c.3280A>C XP_011523635.1:p.Ile1094Leu
XM_011525334.1:c.3280A>C XP_011523636.1:p.Ile1094Leu
XM_011525335.1:c.3220A>C XP_011523637.1:p.Ile1074Leu
XM_011525336.1:c.3160A>C XP_011523638.1:p.Ile1054Leu
XM_011525337.1:c.3079A>C XP_011523639.1:p.Ile1027Leu
XM_011525338.1:c.2797A>C XP_011523640.1:p.Ile933Leu
XM_011525332.3:c.3280A>C XP_011523634.1:p.Ile1094Leu
XM_011525333.3:c.3280A>C XP_011523635.1:p.Ile1094Leu
XM_011525334.2:c.3280A>C XP_011523636.1:p.Ile1094Leu
XM_011525335.3:c.3220A>C XP_011523637.1:p.Ile1074Leu
XM_011525336.2:c.3160A>C XP_011523638.1:p.Ile1054Leu
XM_011525337.2:c.3079A>C XP_011523639.1:p.Ile1027Leu
XM_011525338.2:c.2797A>C XP_011523640.1:p.Ile933Leu
XM_017025200.1:c.2737A>C XP_016880689.1:p.Ile913Leu
XM_017025201.1:c.2737A>C XP_016880690.1:p.Ile913Leu
XM_017025202.1:c.1366A>C XP_016880691.1:p.Ile456Leu
XM_017025203.1:c.1366A>C XP_016880692.1:p.Ile456Leu
NM_032043.3:c.3220A>C MANE Select NP_114432.2:p.Ile1074Leu