Canonical Allele Identifier: CA400479442

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144085714
• MyVariant Identifiers: chr17:g.59761234A>T (hg19) ; chr17:g.61683873A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683873A>T , CM000679.2:g.61683873A>T	GRCh38
NC_000017.10:g.59761234A>T , CM000679.1:g.59761234A>T	GRCh37
NC_000017.9:g.57116016A>T	NCBI36
NG_007409.2:g.184687T>A , LRG_300:g.184687T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1913T>A
ENST00000682453.1:c.3173T>A	ENSP00000506943.1:p.Leu1058Gln
ENST00000682477.1:c.*2599T>A	ENSP00000507075.1:n.*2599T>A
ENST00000682589.1:n.9050T>A
ENST00000682755.1:c.2951T>A	ENSP00000507660.1:p.Leu984Gln
ENST00000682989.1:c.*264T>A	ENSP00000507786.1:n.*264T>A
ENST00000683039.1:c.3173T>A	ENSP00000508303.1:p.Leu1058Gln
ENST00000683235.1:c.*588T>A	ENSP00000507646.1:n.*588T>A
ENST00000683535.1:n.1303T>A
ENST00000684584.1:c.2336T>A	ENSP00000508044.1:p.Leu779Gln
ENST00000684626.1:n.1419T>A
ENST00000684769.1:c.1363T>A	ENSP00000507691.1:n.1363T>A
ENST00000259008.7:c.3173T>A MANE Select	ENSP00000259008.2:p.Leu1058Gln
ENST00000259008.6:c.3173T>A	ENSP00000259008.2:p.Leu1058Gln
NM_032043.2:c.3173T>A , LRG_300t1:c.3173T>A	NP_114432.2:p.Leu1058Gln
XM_011525332.1:c.3233T>A	XP_011523634.1:p.Leu1078Gln
XM_011525333.1:c.3233T>A	XP_011523635.1:p.Leu1078Gln
XM_011525334.1:c.3233T>A	XP_011523636.1:p.Leu1078Gln
XM_011525335.1:c.3173T>A	XP_011523637.1:p.Leu1058Gln
XM_011525336.1:c.3113T>A	XP_011523638.1:p.Leu1038Gln
XM_011525337.1:c.3032T>A	XP_011523639.1:p.Leu1011Gln
XM_011525338.1:c.2750T>A	XP_011523640.1:p.Leu917Gln
XM_011525332.3:c.3233T>A	XP_011523634.1:p.Leu1078Gln
XM_011525333.3:c.3233T>A	XP_011523635.1:p.Leu1078Gln
XM_011525334.2:c.3233T>A	XP_011523636.1:p.Leu1078Gln
XM_011525335.3:c.3173T>A	XP_011523637.1:p.Leu1058Gln
XM_011525336.2:c.3113T>A	XP_011523638.1:p.Leu1038Gln
XM_011525337.2:c.3032T>A	XP_011523639.1:p.Leu1011Gln
XM_011525338.2:c.2750T>A	XP_011523640.1:p.Leu917Gln
XM_017025200.1:c.2690T>A	XP_016880689.1:p.Leu897Gln
XM_017025201.1:c.2690T>A	XP_016880690.1:p.Leu897Gln
XM_017025202.1:c.1319T>A	XP_016880691.1:p.Leu440Gln
XM_017025203.1:c.1319T>A	XP_016880692.1:p.Leu440Gln
NM_032043.3:c.3173T>A MANE Select	NP_114432.2:p.Leu1058Gln