Canonical Allele Identifier: CA2269170287

Gene: BRIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61780337A= , CM000679.2:g.61780337A=	GRCh38
NC_000017.10:g.59857698A= , CM000679.1:g.59857698A=	GRCh37
NC_000017.9:g.57212480A=	NCBI36
NG_007409.2:g.88223T= , LRG_300:g.88223T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000579028.2:c.1441T=	ENSP00000463827.2:n.1441T=
ENST00000584322.2:c.1859T=	ENSP00000463272.2:p.Met620=
ENST00000682066.1:c.1352T=	ENSP00000507191.1:p.Met451=
ENST00000682073.1:n.599T=
ENST00000682453.1:c.1859T=	ENSP00000506943.1:p.Met620=
ENST00000682477.1:c.*1285T=	ENSP00000507075.1:n.*1285T=
ENST00000682589.1:n.4038T=
ENST00000682611.1:c.1352T=	ENSP00000508326.1:p.Met451=
ENST00000682755.1:c.1637T=	ENSP00000507660.1:p.Met546=
ENST00000682989.1:c.1859T=	ENSP00000507786.1:p.Met620=
ENST00000683039.1:c.1859T=	ENSP00000508303.1:p.Met620=
ENST00000683235.1:c.1859T=	ENSP00000507646.1:p.Met620=
ENST00000683381.1:c.1859T=	ENSP00000508184.1:p.Met620=
ENST00000684471.1:n.332T=
ENST00000684584.1:c.1352T=	ENSP00000508044.1:p.Met451=
ENST00000259008.7:c.1859T= MANE Select	ENSP00000259008.2:p.Met620=
ENST00000259008.6:c.1859T=	ENSP00000259008.2:p.Met620=
ENST00000577598.5:c.1859T=	ENSP00000464654.1:p.Met620=
ENST00000579028.1:c.552T=
NM_032043.2:c.1859T= , LRG_300t1:c.1859T=	NP_114432.2:p.Met620=
XM_011525332.1:c.1859T=	XP_011523634.1:p.Met620=
XM_011525333.1:c.1859T=	XP_011523635.1:p.Met620=
XM_011525334.1:c.1859T=	XP_011523636.1:p.Met620=
XM_011525335.1:c.1859T=	XP_011523637.1:p.Met620=
XM_011525336.1:c.1859T=	XP_011523638.1:p.Met620=
XM_011525337.1:c.1794+503T=	XP_011523639.1:n.1794+503T=
XM_011525338.1:c.1376T=	XP_011523640.1:p.Met459=
XM_011525339.1:c.1859T=	XP_011523641.1:p.Met620=
XM_011525340.1:c.1859T=	XP_011523642.1:p.Met620=
XM_011525341.1:c.1859T=	XP_011523643.1:p.Met620=
XM_011525332.3:c.1859T=	XP_011523634.1:p.Met620=
XM_011525333.3:c.1859T=	XP_011523635.1:p.Met620=
XM_011525334.2:c.1859T=	XP_011523636.1:p.Met620=
XM_011525335.3:c.1859T=	XP_011523637.1:p.Met620=
XM_011525336.2:c.1859T=	XP_011523638.1:p.Met620=
XM_011525337.2:c.1794+503T=	XP_011523639.1:n.1794+503T=
XM_011525338.2:c.1376T=	XP_011523640.1:p.Met459=
XM_011525339.3:c.1859T=	XP_011523641.1:p.Met620=
XM_011525340.3:c.1859T=	XP_011523642.1:p.Met620=
XM_011525341.3:c.1859T=	XP_011523643.1:p.Met620=
XM_017025200.1:c.1376T=	XP_016880689.1:p.Met459=
XM_017025201.1:c.1316T=	XP_016880690.1:p.Met439=
XM_017025203.1:c.-102T=	XP_016880692.1:n.-102T=
NM_032043.3:c.1859T= MANE Select	NP_114432.2:p.Met620=