Canonical Allele Identifier: CA400478229

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59760840A>T (hg19) ; chr17:g.61683479A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683479A>T , CM000679.2:g.61683479A>T	GRCh38
NC_000017.10:g.59760840A>T , CM000679.1:g.59760840A>T	GRCh37
NC_000017.9:g.57115622A>T	NCBI36
NG_007409.2:g.185081T>A , LRG_300:g.185081T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2307T>A
ENST00000682453.1:c.3567T>A	ENSP00000506943.1:p.Asp1189Glu
ENST00000682477.1:c.*2993T>A	ENSP00000507075.1:n.*2993T>A
ENST00000682589.1:n.9444T>A
ENST00000682755.1:c.3345T>A	ENSP00000507660.1:p.Asp1115Glu
ENST00000682989.1:c.*658T>A	ENSP00000507786.1:n.*658T>A
ENST00000683039.1:c.3567T>A	ENSP00000508303.1:p.Asp1189Glu
ENST00000683235.1:c.*982T>A	ENSP00000507646.1:n.*982T>A
ENST00000683535.1:n.1697T>A
ENST00000684584.1:c.2730T>A	ENSP00000508044.1:p.Asp910Glu
ENST00000684626.1:n.1813T>A
ENST00000684769.1:c.1757T>A	ENSP00000507691.1:n.1757T>A
ENST00000259008.7:c.3567T>A MANE Select	ENSP00000259008.2:p.Asp1189Glu
ENST00000259008.6:c.3567T>A	ENSP00000259008.2:p.Asp1189Glu
NM_032043.2:c.3567T>A , LRG_300t1:c.3567T>A	NP_114432.2:p.Asp1189Glu
XM_011525332.1:c.3627T>A	XP_011523634.1:p.Asp1209Glu
XM_011525333.1:c.3627T>A	XP_011523635.1:p.Asp1209Glu
XM_011525334.1:c.3627T>A	XP_011523636.1:p.Asp1209Glu
XM_011525335.1:c.3567T>A	XP_011523637.1:p.Asp1189Glu
XM_011525336.1:c.3507T>A	XP_011523638.1:p.Asp1169Glu
XM_011525337.1:c.3426T>A	XP_011523639.1:p.Asp1142Glu
XM_011525338.1:c.3144T>A	XP_011523640.1:p.Asp1048Glu
XM_011525332.3:c.3627T>A	XP_011523634.1:p.Asp1209Glu
XM_011525333.3:c.3627T>A	XP_011523635.1:p.Asp1209Glu
XM_011525334.2:c.3627T>A	XP_011523636.1:p.Asp1209Glu
XM_011525335.3:c.3567T>A	XP_011523637.1:p.Asp1189Glu
XM_011525336.2:c.3507T>A	XP_011523638.1:p.Asp1169Glu
XM_011525337.2:c.3426T>A	XP_011523639.1:p.Asp1142Glu
XM_011525338.2:c.3144T>A	XP_011523640.1:p.Asp1048Glu
XM_017025200.1:c.3084T>A	XP_016880689.1:p.Asp1028Glu
XM_017025201.1:c.3084T>A	XP_016880690.1:p.Asp1028Glu
XM_017025202.1:c.1713T>A	XP_016880691.1:p.Asp571Glu
XM_017025203.1:c.1713T>A	XP_016880692.1:p.Asp571Glu
NM_032043.3:c.3567T>A MANE Select	NP_114432.2:p.Asp1189Glu