Canonical Allele Identifier: CA913187792

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683290G>C , CM000679.2:g.61683290G>C	GRCh38
NC_000017.10:g.59760651G>C , CM000679.1:g.59760651G>C	GRCh37
NC_000017.9:g.57115433G>C	NCBI36
NG_007409.2:g.185270C>G , LRG_300:g.185270C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032043.3:c.*6C>G MANE Select	NP_114432.2:n.*6C>G
ENST00000259008.7:c.*6C>G MANE Select	ENSP00000259008.2:n.*6C>G
NM_032043.2:c.*6C>G , LRG_300t1:c.*6C>G	NP_114432.2:n.*6C>G
ENST00000259008.6:c.*6C>G	ENSP00000259008.2:n.*6C>G
ENST00000682073.1:n.2496C>G
ENST00000682453.1:c.*6C>G	ENSP00000506943.1:n.*6C>G
ENST00000682477.1:c.*3182C>G	ENSP00000507075.1:n.*3182C>G
ENST00000682589.1:n.9633C>G
ENST00000682755.1:c.*6C>G	ENSP00000507660.1:n.*6C>G
ENST00000682989.1:c.*847C>G	ENSP00000507786.1:n.*847C>G
ENST00000683039.1:c.*6C>G	ENSP00000508303.1:n.*6C>G
ENST00000683235.1:c.*1171C>G	ENSP00000507646.1:n.*1171C>G
ENST00000683535.1:n.1886C>G
ENST00000684584.1:c.2919C>G	ENSP00000508044.1:n.2919C>G
ENST00000684626.1:n.2002C>G
ENST00000684769.1:c.1946C>G	ENSP00000507691.1:n.1946C>G
XM_011525332.1:c.*6C>G	XP_011523634.1:n.*6C>G
XM_011525332.3:c.*6C>G	XP_011523634.1:n.*6C>G
XM_011525333.1:c.*6C>G	XP_011523635.1:n.*6C>G
XM_011525333.3:c.*6C>G	XP_011523635.1:n.*6C>G
XM_011525334.1:c.*6C>G	XP_011523636.1:n.*6C>G
XM_011525334.2:c.*6C>G	XP_011523636.1:n.*6C>G
XM_011525335.1:c.*6C>G	XP_011523637.1:n.*6C>G
XM_011525335.3:c.*6C>G	XP_011523637.1:n.*6C>G
XM_011525336.1:c.*6C>G	XP_011523638.1:n.*6C>G
XM_011525336.2:c.*6C>G	XP_011523638.1:n.*6C>G
XM_011525337.1:c.*6C>G	XP_011523639.1:n.*6C>G
XM_011525337.2:c.*6C>G	XP_011523639.1:n.*6C>G
XM_011525338.1:c.*6C>G	XP_011523640.1:n.*6C>G
XM_011525338.2:c.*6C>G	XP_011523640.1:n.*6C>G
XM_017025200.1:c.*6C>G	XP_016880689.1:n.*6C>G
XM_017025201.1:c.*6C>G	XP_016880690.1:n.*6C>G
XM_017025202.1:c.*6C>G	XP_016880691.1:n.*6C>G
XM_017025203.1:c.*6C>G	XP_016880692.1:n.*6C>G