Canonical Allele Identifier: CA2580094579

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61684153G>T , CM000679.2:g.61684153G>T	GRCh38
NC_000017.10:g.59761514G>T , CM000679.1:g.59761514G>T	GRCh37
NC_000017.9:g.57116296G>T	NCBI36
NG_007409.2:g.184407C>A , LRG_300:g.184407C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1646-13C>A
ENST00000682453.1:c.2906-13C>A	ENSP00000506943.1:n.2906-13C>A
ENST00000682477.1:c.*2332-13C>A	ENSP00000507075.1:n.*2332-13C>A
ENST00000682589.1:n.8783-13C>A
ENST00000682755.1:c.2684-13C>A	ENSP00000507660.1:n.2684-13C>A
ENST00000682989.1:c.2610-13C>A	ENSP00000507786.1:n.2610-13C>A
ENST00000683039.1:c.2906-13C>A	ENSP00000508303.1:n.2906-13C>A
ENST00000683235.1:c.*321-13C>A	ENSP00000507646.1:n.*321-13C>A
ENST00000683535.1:n.1036-13C>A
ENST00000684584.1:c.2069-13C>A	ENSP00000508044.1:n.2069-13C>A
ENST00000684626.1:n.1152-13C>A
ENST00000684769.1:c.1096-13C>A	ENSP00000507691.1:n.1096-13C>A
ENST00000259008.7:c.2906-13C>A MANE Select	ENSP00000259008.2:n.2906-13C>A
ENST00000259008.6:c.2906-13C>A	ENSP00000259008.2:n.2906-13C>A
NM_032043.2:c.2906-13C>A , LRG_300t1:c.2906-13C>A	NP_114432.2:n.2906-13C>A
XM_011525332.1:c.2966-13C>A	XP_011523634.1:n.2966-13C>A
XM_011525333.1:c.2966-13C>A	XP_011523635.1:n.2966-13C>A
XM_011525334.1:c.2966-13C>A	XP_011523636.1:n.2966-13C>A
XM_011525335.1:c.2906-13C>A	XP_011523637.1:n.2906-13C>A
XM_011525336.1:c.2846-13C>A	XP_011523638.1:n.2846-13C>A
XM_011525337.1:c.2765-13C>A	XP_011523639.1:n.2765-13C>A
XM_011525338.1:c.2483-13C>A	XP_011523640.1:n.2483-13C>A
XM_011525332.3:c.2966-13C>A	XP_011523634.1:n.2966-13C>A
XM_011525333.3:c.2966-13C>A	XP_011523635.1:n.2966-13C>A
XM_011525334.2:c.2966-13C>A	XP_011523636.1:n.2966-13C>A
XM_011525335.3:c.2906-13C>A	XP_011523637.1:n.2906-13C>A
XM_011525336.2:c.2846-13C>A	XP_011523638.1:n.2846-13C>A
XM_011525337.2:c.2765-13C>A	XP_011523639.1:n.2765-13C>A
XM_011525338.2:c.2483-13C>A	XP_011523640.1:n.2483-13C>A
XM_017025200.1:c.2423-13C>A	XP_016880689.1:n.2423-13C>A
XM_017025201.1:c.2423-13C>A	XP_016880690.1:n.2423-13C>A
XM_017025202.1:c.1052-13C>A	XP_016880691.1:n.1052-13C>A
XM_017025203.1:c.1052-13C>A	XP_016880692.1:n.1052-13C>A
NM_032043.3:c.2906-13C>A MANE Select	NP_114432.2:n.2906-13C>A