Canonical Allele Identifier: CA2269131921

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61685986A= , CM000679.2:g.61685986A=	GRCh38
NC_000017.10:g.59763347A= , CM000679.1:g.59763347A=	GRCh37
NC_000017.9:g.57118129A=	NCBI36
NG_007409.2:g.182574T= , LRG_300:g.182574T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000682066.1:c.2885T=	ENSP00000507191.1:n.2885T=
ENST00000682073.1:n.1495T=
ENST00000682433.1:n.1834T=
ENST00000682453.1:c.2755T=	ENSP00000506943.1:p.Ser919=
ENST00000682477.1:c.*2181T=	ENSP00000507075.1:n.*2181T=
ENST00000682589.1:n.8632T=
ENST00000682755.1:c.2533T=	ENSP00000507660.1:p.Ser845=
ENST00000682989.1:c.2610-1846T=	ENSP00000507786.1:n.2610-1846T=
ENST00000683039.1:c.2755T=	ENSP00000508303.1:p.Ser919=
ENST00000683235.1:c.*170T=	ENSP00000507646.1:n.*170T=
ENST00000683535.1:n.885T=
ENST00000684471.1:n.1168T=
ENST00000684584.1:c.2069-1846T=	ENSP00000508044.1:n.2069-1846T=
ENST00000684626.1:n.1001T=
ENST00000684769.1:c.945T=	ENSP00000507691.1:n.945T=
ENST00000259008.7:c.2755T= MANE Select	ENSP00000259008.2:p.Ser919=
ENST00000259008.6:c.2755T=	ENSP00000259008.2:p.Ser919=
ENST00000577598.5:c.2755T=	ENSP00000464654.1:p.Ser919=
NM_032043.2:c.2755T= , LRG_300t1:c.2755T=	NP_114432.2:p.Ser919=
XM_011525332.1:c.2815T=	XP_011523634.1:p.Ser939=
XM_011525333.1:c.2815T=	XP_011523635.1:p.Ser939=
XM_011525334.1:c.2815T=	XP_011523636.1:p.Ser939=
XM_011525335.1:c.2755T=	XP_011523637.1:p.Ser919=
XM_011525336.1:c.2695T=	XP_011523638.1:p.Ser899=
XM_011525337.1:c.2614T=	XP_011523639.1:p.Ser872=
XM_011525338.1:c.2332T=	XP_011523640.1:p.Ser778=
XM_011525332.3:c.2815T=	XP_011523634.1:p.Ser939=
XM_011525333.3:c.2815T=	XP_011523635.1:p.Ser939=
XM_011525334.2:c.2815T=	XP_011523636.1:p.Ser939=
XM_011525335.3:c.2755T=	XP_011523637.1:p.Ser919=
XM_011525336.2:c.2695T=	XP_011523638.1:p.Ser899=
XM_011525337.2:c.2614T=	XP_011523639.1:p.Ser872=
XM_011525338.2:c.2332T=	XP_011523640.1:p.Ser778=
XM_017025200.1:c.2272T=	XP_016880689.1:p.Ser758=
XM_017025201.1:c.2272T=	XP_016880690.1:p.Ser758=
XM_017025202.1:c.901T=	XP_016880691.1:p.Ser301=
XM_017025203.1:c.901T=	XP_016880692.1:p.Ser301=
NM_032043.3:c.2755T= MANE Select	NP_114432.2:p.Ser919=