Canonical Allele Identifier: CA400483033
Community Standard Title: NM_032043.3(BRIP1):c.2194A>T (p.Lys732Ter)
Gene: BRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61744495T>A , CM000679.2:g.61744495T>A GRCh38
NC_000017.10:g.59821856T>A , CM000679.1:g.59821856T>A GRCh37
NC_000017.9:g.57176638T>A NCBI36
NG_007409.2:g.124065A>T , LRG_300:g.124065A>T

Transcript Alleles

HGVS Amino-acid Change
NM_032043.3:c.2194A>T MANE Select NP_114432.2:p.Lys732Ter
ENST00000259008.7:c.2194A>T MANE Select ENSP00000259008.2:p.Lys732Ter
NM_032043.2:c.2194A>T , LRG_300t1:c.2194A>T NP_114432.2:p.Lys732Ter
ENST00000259008.6:c.2194A>T ENSP00000259008.2:p.Lys732Ter
ENST00000577598.5:c.2194A>T ENSP00000464654.1:p.Lys732Ter
ENST00000579028.2:c.1776A>T ENSP00000463827.2:n.1776A>T
ENST00000584322.1:c.177A>T
ENST00000584322.2:c.2194A>T ENSP00000463272.2:p.Lys732Ter
ENST00000682066.1:c.2324A>T ENSP00000507191.1:n.2324A>T
ENST00000682073.1:n.934A>T
ENST00000682433.1:n.1273A>T
ENST00000682453.1:c.2194A>T ENSP00000506943.1:p.Lys732Ter
ENST00000682477.1:c.*1620A>T ENSP00000507075.1:n.*1620A>T
ENST00000682589.1:n.8071A>T
ENST00000682755.1:c.1972A>T ENSP00000507660.1:p.Lys658Ter
ENST00000682989.1:c.2194A>T ENSP00000507786.1:p.Lys732Ter
ENST00000683039.1:c.2194A>T ENSP00000508303.1:p.Lys732Ter
ENST00000683235.1:c.2194A>T ENSP00000507646.1:p.Lys732Ter
ENST00000683381.1:c.2254A>T ENSP00000508184.1:p.Lys752Ter
ENST00000683535.1:n.324A>T
ENST00000684471.1:n.607A>T
ENST00000684584.1:c.1687A>T ENSP00000508044.1:p.Lys563Ter
ENST00000684769.1:c.259A>T ENSP00000507691.1:p.Lys87Ter
XM_011525332.1:c.2254A>T XP_011523634.1:p.Lys752Ter
XM_011525332.3:c.2254A>T XP_011523634.1:p.Lys752Ter
XM_011525333.1:c.2254A>T XP_011523635.1:p.Lys752Ter
XM_011525333.3:c.2254A>T XP_011523635.1:p.Lys752Ter
XM_011525334.1:c.2254A>T XP_011523636.1:p.Lys752Ter
XM_011525334.2:c.2254A>T XP_011523636.1:p.Lys752Ter
XM_011525335.1:c.2194A>T XP_011523637.1:p.Lys732Ter
XM_011525335.3:c.2194A>T XP_011523637.1:p.Lys732Ter
XM_011525336.1:c.2134A>T XP_011523638.1:p.Lys712Ter
XM_011525336.2:c.2134A>T XP_011523638.1:p.Lys712Ter
XM_011525337.1:c.2053A>T XP_011523639.1:p.Lys685Ter
XM_011525337.2:c.2053A>T XP_011523639.1:p.Lys685Ter
XM_011525338.1:c.1771A>T XP_011523640.1:p.Lys591Ter
XM_011525338.2:c.1771A>T XP_011523640.1:p.Lys591Ter
XM_011525339.1:c.2254A>T XP_011523641.1:p.Lys752Ter
XM_011525339.3:c.2254A>T XP_011523641.1:p.Lys752Ter
XM_011525340.1:c.2254A>T XP_011523642.1:p.Lys752Ter
XM_011525340.3:c.2254A>T XP_011523642.1:p.Lys752Ter
XM_017025200.1:c.1711A>T XP_016880689.1:p.Lys571Ter
XM_017025201.1:c.1711A>T XP_016880690.1:p.Lys571Ter
XM_017025202.1:c.340A>T XP_016880691.1:p.Lys114Ter
XM_017025203.1:c.340A>T XP_016880692.1:p.Lys114Ter