Canonical Allele Identifier: CA400478555

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144074052
• MyVariant Identifiers: chr17:g.59760916C>T (hg19) ; chr17:g.61683555C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683555C>T , CM000679.2:g.61683555C>T	GRCh38
NC_000017.10:g.59760916C>T , CM000679.1:g.59760916C>T	GRCh37
NC_000017.9:g.57115698C>T	NCBI36
NG_007409.2:g.185005G>A , LRG_300:g.185005G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2231G>A
ENST00000682453.1:c.3491G>A	ENSP00000506943.1:p.Cys1164Tyr
ENST00000682477.1:c.*2917G>A	ENSP00000507075.1:n.*2917G>A
ENST00000682589.1:n.9368G>A
ENST00000682755.1:c.3269G>A	ENSP00000507660.1:p.Cys1090Tyr
ENST00000682989.1:c.*582G>A	ENSP00000507786.1:n.*582G>A
ENST00000683039.1:c.3491G>A	ENSP00000508303.1:p.Cys1164Tyr
ENST00000683235.1:c.*906G>A	ENSP00000507646.1:n.*906G>A
ENST00000683535.1:n.1621G>A
ENST00000684584.1:c.2654G>A	ENSP00000508044.1:p.Cys885Tyr
ENST00000684626.1:n.1737G>A
ENST00000684769.1:c.1681G>A	ENSP00000507691.1:n.1681G>A
ENST00000259008.7:c.3491G>A MANE Select	ENSP00000259008.2:p.Cys1164Tyr
ENST00000259008.6:c.3491G>A	ENSP00000259008.2:p.Cys1164Tyr
NM_032043.2:c.3491G>A , LRG_300t1:c.3491G>A	NP_114432.2:p.Cys1164Tyr
XM_011525332.1:c.3551G>A	XP_011523634.1:p.Cys1184Tyr
XM_011525333.1:c.3551G>A	XP_011523635.1:p.Cys1184Tyr
XM_011525334.1:c.3551G>A	XP_011523636.1:p.Cys1184Tyr
XM_011525335.1:c.3491G>A	XP_011523637.1:p.Cys1164Tyr
XM_011525336.1:c.3431G>A	XP_011523638.1:p.Cys1144Tyr
XM_011525337.1:c.3350G>A	XP_011523639.1:p.Cys1117Tyr
XM_011525338.1:c.3068G>A	XP_011523640.1:p.Cys1023Tyr
XM_011525332.3:c.3551G>A	XP_011523634.1:p.Cys1184Tyr
XM_011525333.3:c.3551G>A	XP_011523635.1:p.Cys1184Tyr
XM_011525334.2:c.3551G>A	XP_011523636.1:p.Cys1184Tyr
XM_011525335.3:c.3491G>A	XP_011523637.1:p.Cys1164Tyr
XM_011525336.2:c.3431G>A	XP_011523638.1:p.Cys1144Tyr
XM_011525337.2:c.3350G>A	XP_011523639.1:p.Cys1117Tyr
XM_011525338.2:c.3068G>A	XP_011523640.1:p.Cys1023Tyr
XM_017025200.1:c.3008G>A	XP_016880689.1:p.Cys1003Tyr
XM_017025201.1:c.3008G>A	XP_016880690.1:p.Cys1003Tyr
XM_017025202.1:c.1637G>A	XP_016880691.1:p.Cys546Tyr
XM_017025203.1:c.1637G>A	XP_016880692.1:p.Cys546Tyr
NM_032043.3:c.3491G>A MANE Select	NP_114432.2:p.Cys1164Tyr