Canonical Allele Identifier: CA2269131932
Gene: BRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61685997T= , CM000679.2:g.61685997T= GRCh38
NC_000017.10:g.59763358T= , CM000679.1:g.59763358T= GRCh37
NC_000017.9:g.57118140T= NCBI36
NG_007409.2:g.182563A= , LRG_300:g.182563A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682066.1:c.2874A= ENSP00000507191.1:n.2874A=
ENST00000682073.1:n.1484A=
ENST00000682433.1:n.1823A=
ENST00000682453.1:c.2744A= ENSP00000506943.1:p.Lys915=
ENST00000682477.1:c.*2170A= ENSP00000507075.1:n.*2170A=
ENST00000682589.1:n.8621A=
ENST00000682755.1:c.2522A= ENSP00000507660.1:p.Lys841=
ENST00000682989.1:c.2610-1857A= ENSP00000507786.1:n.2610-1857A=
ENST00000683039.1:c.2744A= ENSP00000508303.1:p.Lys915=
ENST00000683235.1:c.*159A= ENSP00000507646.1:n.*159A=
ENST00000683535.1:n.874A=
ENST00000684471.1:n.1157A=
ENST00000684584.1:c.2069-1857A= ENSP00000508044.1:n.2069-1857A=
ENST00000684626.1:n.990A=
ENST00000684769.1:c.934A= ENSP00000507691.1:n.934A=
ENST00000259008.7:c.2744A= MANE Select ENSP00000259008.2:p.Lys915=
ENST00000259008.6:c.2744A= ENSP00000259008.2:p.Lys915=
ENST00000577598.5:c.2744A= ENSP00000464654.1:p.Lys915=
NM_032043.2:c.2744A= , LRG_300t1:c.2744A= NP_114432.2:p.Lys915=
XM_011525332.1:c.2804A= XP_011523634.1:p.Lys935=
XM_011525333.1:c.2804A= XP_011523635.1:p.Lys935=
XM_011525334.1:c.2804A= XP_011523636.1:p.Lys935=
XM_011525335.1:c.2744A= XP_011523637.1:p.Lys915=
XM_011525336.1:c.2684A= XP_011523638.1:p.Lys895=
XM_011525337.1:c.2603A= XP_011523639.1:p.Lys868=
XM_011525338.1:c.2321A= XP_011523640.1:p.Lys774=
XM_011525332.3:c.2804A= XP_011523634.1:p.Lys935=
XM_011525333.3:c.2804A= XP_011523635.1:p.Lys935=
XM_011525334.2:c.2804A= XP_011523636.1:p.Lys935=
XM_011525335.3:c.2744A= XP_011523637.1:p.Lys915=
XM_011525336.2:c.2684A= XP_011523638.1:p.Lys895=
XM_011525337.2:c.2603A= XP_011523639.1:p.Lys868=
XM_011525338.2:c.2321A= XP_011523640.1:p.Lys774=
XM_017025200.1:c.2261A= XP_016880689.1:p.Lys754=
XM_017025201.1:c.2261A= XP_016880690.1:p.Lys754=
XM_017025202.1:c.890A= XP_016880691.1:p.Lys297=
XM_017025203.1:c.890A= XP_016880692.1:p.Lys297=
NM_032043.3:c.2744A= MANE Select NP_114432.2:p.Lys915=