Canonical Allele Identifier: CA400481674
Community Standard Title: NM_032043.3(BRIP1):c.2716G>T (p.Glu906Ter)
Gene: BRIP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61686025C>A , CM000679.2:g.61686025C>A GRCh38
NC_000017.10:g.59763386C>A , CM000679.1:g.59763386C>A GRCh37
NC_000017.9:g.57118168C>A NCBI36
NG_007409.2:g.182535G>T , LRG_300:g.182535G>T

Transcript Alleles

HGVS Amino-acid Change
NM_032043.3:c.2716G>T MANE Select NP_114432.2:p.Glu906Ter
ENST00000259008.7:c.2716G>T MANE Select ENSP00000259008.2:p.Glu906Ter
NM_032043.2:c.2716G>T , LRG_300t1:c.2716G>T NP_114432.2:p.Glu906Ter
ENST00000259008.6:c.2716G>T ENSP00000259008.2:p.Glu906Ter
ENST00000577598.5:c.2716G>T ENSP00000464654.1:p.Glu906Ter
ENST00000682066.1:c.2846G>T ENSP00000507191.1:n.2846G>T
ENST00000682073.1:n.1456G>T
ENST00000682433.1:n.1795G>T
ENST00000682453.1:c.2716G>T ENSP00000506943.1:p.Glu906Ter
ENST00000682477.1:c.*2142G>T ENSP00000507075.1:n.*2142G>T
ENST00000682589.1:n.8593G>T
ENST00000682755.1:c.2494G>T ENSP00000507660.1:p.Glu832Ter
ENST00000682989.1:c.2610-1885G>T ENSP00000507786.1:n.2610-1885G>T
ENST00000683039.1:c.2716G>T ENSP00000508303.1:p.Glu906Ter
ENST00000683235.1:c.*131G>T ENSP00000507646.1:n.*131G>T
ENST00000683535.1:n.846G>T
ENST00000684471.1:n.1129G>T
ENST00000684584.1:c.2069-1885G>T ENSP00000508044.1:n.2069-1885G>T
ENST00000684626.1:n.962G>T
ENST00000684769.1:c.906G>T ENSP00000507691.1:n.906G>T
XM_011525332.1:c.2776G>T XP_011523634.1:p.Glu926Ter
XM_011525332.3:c.2776G>T XP_011523634.1:p.Glu926Ter
XM_011525333.1:c.2776G>T XP_011523635.1:p.Glu926Ter
XM_011525333.3:c.2776G>T XP_011523635.1:p.Glu926Ter
XM_011525334.1:c.2776G>T XP_011523636.1:p.Glu926Ter
XM_011525334.2:c.2776G>T XP_011523636.1:p.Glu926Ter
XM_011525335.1:c.2716G>T XP_011523637.1:p.Glu906Ter
XM_011525335.3:c.2716G>T XP_011523637.1:p.Glu906Ter
XM_011525336.1:c.2656G>T XP_011523638.1:p.Glu886Ter
XM_011525336.2:c.2656G>T XP_011523638.1:p.Glu886Ter
XM_011525337.1:c.2575G>T XP_011523639.1:p.Glu859Ter
XM_011525337.2:c.2575G>T XP_011523639.1:p.Glu859Ter
XM_011525338.1:c.2293G>T XP_011523640.1:p.Glu765Ter
XM_011525338.2:c.2293G>T XP_011523640.1:p.Glu765Ter
XM_017025200.1:c.2233G>T XP_016880689.1:p.Glu745Ter
XM_017025201.1:c.2233G>T XP_016880690.1:p.Glu745Ter
XM_017025202.1:c.862G>T XP_016880691.1:p.Glu288Ter
XM_017025203.1:c.862G>T XP_016880692.1:p.Glu288Ter