Canonical Allele Identifier: CA400479113
Gene: BRIP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61683788T>G , CM000679.2:g.61683788T>G GRCh38
NC_000017.10:g.59761149T>G , CM000679.1:g.59761149T>G GRCh37
NC_000017.9:g.57115931T>G NCBI36
NG_007409.2:g.184772A>C , LRG_300:g.184772A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682073.1:n.1998A>C
ENST00000682453.1:c.3258A>C ENSP00000506943.1:p.Lys1086Asn
ENST00000682477.1:c.*2684A>C ENSP00000507075.1:n.*2684A>C
ENST00000682589.1:n.9135A>C
ENST00000682755.1:c.3036A>C ENSP00000507660.1:p.Lys1012Asn
ENST00000682989.1:c.*349A>C ENSP00000507786.1:n.*349A>C
ENST00000683039.1:c.3258A>C ENSP00000508303.1:p.Lys1086Asn
ENST00000683235.1:c.*673A>C ENSP00000507646.1:n.*673A>C
ENST00000683535.1:n.1388A>C
ENST00000684584.1:c.2421A>C ENSP00000508044.1:p.Lys807Asn
ENST00000684626.1:n.1504A>C
ENST00000684769.1:c.1448A>C ENSP00000507691.1:n.1448A>C
ENST00000259008.7:c.3258A>C MANE Select ENSP00000259008.2:p.Lys1086Asn
ENST00000259008.6:c.3258A>C ENSP00000259008.2:p.Lys1086Asn
NM_032043.2:c.3258A>C , LRG_300t1:c.3258A>C NP_114432.2:p.Lys1086Asn
XM_011525332.1:c.3318A>C XP_011523634.1:p.Lys1106Asn
XM_011525333.1:c.3318A>C XP_011523635.1:p.Lys1106Asn
XM_011525334.1:c.3318A>C XP_011523636.1:p.Lys1106Asn
XM_011525335.1:c.3258A>C XP_011523637.1:p.Lys1086Asn
XM_011525336.1:c.3198A>C XP_011523638.1:p.Lys1066Asn
XM_011525337.1:c.3117A>C XP_011523639.1:p.Lys1039Asn
XM_011525338.1:c.2835A>C XP_011523640.1:p.Lys945Asn
XM_011525332.3:c.3318A>C XP_011523634.1:p.Lys1106Asn
XM_011525333.3:c.3318A>C XP_011523635.1:p.Lys1106Asn
XM_011525334.2:c.3318A>C XP_011523636.1:p.Lys1106Asn
XM_011525335.3:c.3258A>C XP_011523637.1:p.Lys1086Asn
XM_011525336.2:c.3198A>C XP_011523638.1:p.Lys1066Asn
XM_011525337.2:c.3117A>C XP_011523639.1:p.Lys1039Asn
XM_011525338.2:c.2835A>C XP_011523640.1:p.Lys945Asn
XM_017025200.1:c.2775A>C XP_016880689.1:p.Lys925Asn
XM_017025201.1:c.2775A>C XP_016880690.1:p.Lys925Asn
XM_017025202.1:c.1404A>C XP_016880691.1:p.Lys468Asn
XM_017025203.1:c.1404A>C XP_016880692.1:p.Lys468Asn
NM_032043.3:c.3258A>C MANE Select NP_114432.2:p.Lys1086Asn