Canonical Allele Identifier: CA400478471

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59760895A>C (hg19) ; chr17:g.61683534A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683534A>C , CM000679.2:g.61683534A>C	GRCh38
NC_000017.10:g.59760895A>C , CM000679.1:g.59760895A>C	GRCh37
NC_000017.9:g.57115677A>C	NCBI36
NG_007409.2:g.185026T>G , LRG_300:g.185026T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2252T>G
ENST00000682453.1:c.3512T>G	ENSP00000506943.1:p.Phe1171Cys
ENST00000682477.1:c.*2938T>G	ENSP00000507075.1:n.*2938T>G
ENST00000682589.1:n.9389T>G
ENST00000682755.1:c.3290T>G	ENSP00000507660.1:p.Phe1097Cys
ENST00000682989.1:c.*603T>G	ENSP00000507786.1:n.*603T>G
ENST00000683039.1:c.3512T>G	ENSP00000508303.1:p.Phe1171Cys
ENST00000683235.1:c.*927T>G	ENSP00000507646.1:n.*927T>G
ENST00000683535.1:n.1642T>G
ENST00000684584.1:c.2675T>G	ENSP00000508044.1:p.Phe892Cys
ENST00000684626.1:n.1758T>G
ENST00000684769.1:c.1702T>G	ENSP00000507691.1:n.1702T>G
ENST00000259008.7:c.3512T>G MANE Select	ENSP00000259008.2:p.Phe1171Cys
ENST00000259008.6:c.3512T>G	ENSP00000259008.2:p.Phe1171Cys
NM_032043.2:c.3512T>G , LRG_300t1:c.3512T>G	NP_114432.2:p.Phe1171Cys
XM_011525332.1:c.3572T>G	XP_011523634.1:p.Phe1191Cys
XM_011525333.1:c.3572T>G	XP_011523635.1:p.Phe1191Cys
XM_011525334.1:c.3572T>G	XP_011523636.1:p.Phe1191Cys
XM_011525335.1:c.3512T>G	XP_011523637.1:p.Phe1171Cys
XM_011525336.1:c.3452T>G	XP_011523638.1:p.Phe1151Cys
XM_011525337.1:c.3371T>G	XP_011523639.1:p.Phe1124Cys
XM_011525338.1:c.3089T>G	XP_011523640.1:p.Phe1030Cys
XM_011525332.3:c.3572T>G	XP_011523634.1:p.Phe1191Cys
XM_011525333.3:c.3572T>G	XP_011523635.1:p.Phe1191Cys
XM_011525334.2:c.3572T>G	XP_011523636.1:p.Phe1191Cys
XM_011525335.3:c.3512T>G	XP_011523637.1:p.Phe1171Cys
XM_011525336.2:c.3452T>G	XP_011523638.1:p.Phe1151Cys
XM_011525337.2:c.3371T>G	XP_011523639.1:p.Phe1124Cys
XM_011525338.2:c.3089T>G	XP_011523640.1:p.Phe1030Cys
XM_017025200.1:c.3029T>G	XP_016880689.1:p.Phe1010Cys
XM_017025201.1:c.3029T>G	XP_016880690.1:p.Phe1010Cys
XM_017025202.1:c.1658T>G	XP_016880691.1:p.Phe553Cys
XM_017025203.1:c.1658T>G	XP_016880692.1:p.Phe553Cys
NM_032043.3:c.3512T>G MANE Select	NP_114432.2:p.Phe1171Cys