Canonical Allele Identifier: CA2269161180
Gene: BRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61758726T= , CM000679.2:g.61758726T= GRCh38
NC_000017.10:g.59836087T= , CM000679.1:g.59836087T= GRCh37
NC_000017.9:g.57190869T= NCBI36
NG_007409.2:g.109834A= , LRG_300:g.109834A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000579028.2:c.1680-14135A= ENSP00000463827.2:n.1680-14135A=
ENST00000584322.2:c.2098-14135A= ENSP00000463272.2:n.2098-14135A=
ENST00000682066.1:c.2175A= ENSP00000507191.1:n.2175A=
ENST00000682073.1:n.838-14135A=
ENST00000682433.1:n.1177-14135A=
ENST00000682453.1:c.2098-14135A= ENSP00000506943.1:n.2098-14135A=
ENST00000682477.1:c.*1524-14135A= ENSP00000507075.1:n.*1524-14135A=
ENST00000682589.1:n.7975-14135A=
ENST00000682755.1:c.1876-14135A= ENSP00000507660.1:n.1876-14135A=
ENST00000682989.1:c.2098-14135A= ENSP00000507786.1:n.2098-14135A=
ENST00000683039.1:c.2098-14135A= ENSP00000508303.1:n.2098-14135A=
ENST00000683235.1:c.2098-14135A= ENSP00000507646.1:n.2098-14135A=
ENST00000683381.1:c.2158-14135A= ENSP00000508184.1:n.2158-14135A=
ENST00000683535.1:n.228-14135A=
ENST00000684471.1:n.511-14135A=
ENST00000684584.1:c.1591-14135A= ENSP00000508044.1:n.1591-14135A=
ENST00000684769.1:c.163-14135A= ENSP00000507691.1:n.163-14135A=
ENST00000259008.7:c.2098-14135A= MANE Select ENSP00000259008.2:n.2098-14135A=
ENST00000259008.6:c.2098-14135A= ENSP00000259008.2:n.2098-14135A=
ENST00000577598.5:c.2098-14135A= ENSP00000464654.1:n.2098-14135A=
ENST00000584322.1:c.81-14135A=
NM_032043.2:c.2098-14135A= , LRG_300t1:c.2098-14135A= NP_114432.2:n.2098-14135A=
XM_011525332.1:c.2158-14135A= XP_011523634.1:n.2158-14135A=
XM_011525333.1:c.2158-14135A= XP_011523635.1:n.2158-14135A=
XM_011525334.1:c.2158-14135A= XP_011523636.1:n.2158-14135A=
XM_011525335.1:c.2098-14135A= XP_011523637.1:n.2098-14135A=
XM_011525336.1:c.2038-14135A= XP_011523638.1:n.2038-14135A=
XM_011525337.1:c.1957-14135A= XP_011523639.1:n.1957-14135A=
XM_011525338.1:c.1675-14135A= XP_011523640.1:n.1675-14135A=
XM_011525339.1:c.2158-14135A= XP_011523641.1:n.2158-14135A=
XM_011525340.1:c.2158-14135A= XP_011523642.1:n.2158-14135A=
XM_011525332.3:c.2158-14135A= XP_011523634.1:n.2158-14135A=
XM_011525333.3:c.2158-14135A= XP_011523635.1:n.2158-14135A=
XM_011525334.2:c.2158-14135A= XP_011523636.1:n.2158-14135A=
XM_011525335.3:c.2098-14135A= XP_011523637.1:n.2098-14135A=
XM_011525336.2:c.2038-14135A= XP_011523638.1:n.2038-14135A=
XM_011525337.2:c.1957-14135A= XP_011523639.1:n.1957-14135A=
XM_011525338.2:c.1675-14135A= XP_011523640.1:n.1675-14135A=
XM_011525339.3:c.2158-14135A= XP_011523641.1:n.2158-14135A=
XM_011525340.3:c.2158-14135A= XP_011523642.1:n.2158-14135A=
XM_017025200.1:c.1615-14135A= XP_016880689.1:n.1615-14135A=
XM_017025201.1:c.1615-14135A= XP_016880690.1:n.1615-14135A=
XM_017025202.1:c.244-14135A= XP_016880691.1:n.244-14135A=
XM_017025203.1:c.244-14135A= XP_016880692.1:n.244-14135A=
NM_032043.3:c.2098-14135A= MANE Select NP_114432.2:n.2098-14135A=