Canonical Allele Identifier: CA501335303

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59761212T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683851T>A , CM000679.2:g.61683851T>A	GRCh38
NC_000017.10:g.59761212T>A , CM000679.1:g.59761212T>A	GRCh37
NC_000017.9:g.57115994T>A	NCBI36
NG_007409.2:g.184709A>T , LRG_300:g.184709A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1935A>T
ENST00000682453.1:c.3195A>T	ENSP00000506943.1:p.Gly1065=
ENST00000682477.1:c.*2621A>T	ENSP00000507075.1:n.*2621A>T
ENST00000682589.1:n.9072A>T
ENST00000682755.1:c.2973A>T	ENSP00000507660.1:p.Gly991=
ENST00000682989.1:c.*286A>T	ENSP00000507786.1:n.*286A>T
ENST00000683039.1:c.3195A>T	ENSP00000508303.1:p.Gly1065=
ENST00000683235.1:c.*610A>T	ENSP00000507646.1:n.*610A>T
ENST00000683535.1:n.1325A>T
ENST00000684584.1:c.2358A>T	ENSP00000508044.1:p.Gly786=
ENST00000684626.1:n.1441A>T
ENST00000684769.1:c.1385A>T	ENSP00000507691.1:n.1385A>T
ENST00000259008.7:c.3195A>T MANE Select	ENSP00000259008.2:p.Gly1065=
ENST00000259008.6:c.3195A>T	ENSP00000259008.2:p.Gly1065=
NM_032043.2:c.3195A>T , LRG_300t1:c.3195A>T	NP_114432.2:p.Gly1065=
XM_011525332.1:c.3255A>T	XP_011523634.1:p.Gly1085=
XM_011525333.1:c.3255A>T	XP_011523635.1:p.Gly1085=
XM_011525334.1:c.3255A>T	XP_011523636.1:p.Gly1085=
XM_011525335.1:c.3195A>T	XP_011523637.1:p.Gly1065=
XM_011525336.1:c.3135A>T	XP_011523638.1:p.Gly1045=
XM_011525337.1:c.3054A>T	XP_011523639.1:p.Gly1018=
XM_011525338.1:c.2772A>T	XP_011523640.1:p.Gly924=
XM_011525332.3:c.3255A>T	XP_011523634.1:p.Gly1085=
XM_011525333.3:c.3255A>T	XP_011523635.1:p.Gly1085=
XM_011525334.2:c.3255A>T	XP_011523636.1:p.Gly1085=
XM_011525335.3:c.3195A>T	XP_011523637.1:p.Gly1065=
XM_011525336.2:c.3135A>T	XP_011523638.1:p.Gly1045=
XM_011525337.2:c.3054A>T	XP_011523639.1:p.Gly1018=
XM_011525338.2:c.2772A>T	XP_011523640.1:p.Gly924=
XM_017025200.1:c.2712A>T	XP_016880689.1:p.Gly904=
XM_017025201.1:c.2712A>T	XP_016880690.1:p.Gly904=
XM_017025202.1:c.1341A>T	XP_016880691.1:p.Gly447=
XM_017025203.1:c.1341A>T	XP_016880692.1:p.Gly447=
NM_032043.3:c.3195A>T MANE Select	NP_114432.2:p.Gly1065=