Canonical Allele Identifier: CA400478808

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144077516
• MyVariant Identifiers: chr17:g.59761006G>T (hg19) ; chr17:g.61683645G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683645G>T , CM000679.2:g.61683645G>T	GRCh38
NC_000017.10:g.59761006G>T , CM000679.1:g.59761006G>T	GRCh37
NC_000017.9:g.57115788G>T	NCBI36
NG_007409.2:g.184915C>A , LRG_300:g.184915C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2141C>A
ENST00000682453.1:c.3401C>A	ENSP00000506943.1:p.Pro1134His
ENST00000682477.1:c.*2827C>A	ENSP00000507075.1:n.*2827C>A
ENST00000682589.1:n.9278C>A
ENST00000682755.1:c.3179C>A	ENSP00000507660.1:p.Pro1060His
ENST00000682989.1:c.*492C>A	ENSP00000507786.1:n.*492C>A
ENST00000683039.1:c.3401C>A	ENSP00000508303.1:p.Pro1134His
ENST00000683235.1:c.*816C>A	ENSP00000507646.1:n.*816C>A
ENST00000683535.1:n.1531C>A
ENST00000684584.1:c.2564C>A	ENSP00000508044.1:p.Pro855His
ENST00000684626.1:n.1647C>A
ENST00000684769.1:c.1591C>A	ENSP00000507691.1:n.1591C>A
ENST00000259008.7:c.3401C>A MANE Select	ENSP00000259008.2:p.Pro1134His
ENST00000259008.6:c.3401C>A	ENSP00000259008.2:p.Pro1134His
NM_032043.2:c.3401C>A , LRG_300t1:c.3401C>A	NP_114432.2:p.Pro1134His
XM_011525332.1:c.3461C>A	XP_011523634.1:p.Pro1154His
XM_011525333.1:c.3461C>A	XP_011523635.1:p.Pro1154His
XM_011525334.1:c.3461C>A	XP_011523636.1:p.Pro1154His
XM_011525335.1:c.3401C>A	XP_011523637.1:p.Pro1134His
XM_011525336.1:c.3341C>A	XP_011523638.1:p.Pro1114His
XM_011525337.1:c.3260C>A	XP_011523639.1:p.Pro1087His
XM_011525338.1:c.2978C>A	XP_011523640.1:p.Pro993His
XM_011525332.3:c.3461C>A	XP_011523634.1:p.Pro1154His
XM_011525333.3:c.3461C>A	XP_011523635.1:p.Pro1154His
XM_011525334.2:c.3461C>A	XP_011523636.1:p.Pro1154His
XM_011525335.3:c.3401C>A	XP_011523637.1:p.Pro1134His
XM_011525336.2:c.3341C>A	XP_011523638.1:p.Pro1114His
XM_011525337.2:c.3260C>A	XP_011523639.1:p.Pro1087His
XM_011525338.2:c.2978C>A	XP_011523640.1:p.Pro993His
XM_017025200.1:c.2918C>A	XP_016880689.1:p.Pro973His
XM_017025201.1:c.2918C>A	XP_016880690.1:p.Pro973His
XM_017025202.1:c.1547C>A	XP_016880691.1:p.Pro516His
XM_017025203.1:c.1547C>A	XP_016880692.1:p.Pro516His
NM_032043.3:c.3401C>A MANE Select	NP_114432.2:p.Pro1134His