Canonical Allele Identifier: CA400478518

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144073718
• MyVariant Identifiers: chr17:g.59760907G>C (hg19) ; chr17:g.61683546G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683546G>C , CM000679.2:g.61683546G>C	GRCh38
NC_000017.10:g.59760907G>C , CM000679.1:g.59760907G>C	GRCh37
NC_000017.9:g.57115689G>C	NCBI36
NG_007409.2:g.185014C>G , LRG_300:g.185014C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2240C>G
ENST00000682453.1:c.3500C>G	ENSP00000506943.1:p.Ala1167Gly
ENST00000682477.1:c.*2926C>G	ENSP00000507075.1:n.*2926C>G
ENST00000682589.1:n.9377C>G
ENST00000682755.1:c.3278C>G	ENSP00000507660.1:p.Ala1093Gly
ENST00000682989.1:c.*591C>G	ENSP00000507786.1:n.*591C>G
ENST00000683039.1:c.3500C>G	ENSP00000508303.1:p.Ala1167Gly
ENST00000683235.1:c.*915C>G	ENSP00000507646.1:n.*915C>G
ENST00000683535.1:n.1630C>G
ENST00000684584.1:c.2663C>G	ENSP00000508044.1:p.Ala888Gly
ENST00000684626.1:n.1746C>G
ENST00000684769.1:c.1690C>G	ENSP00000507691.1:n.1690C>G
ENST00000259008.7:c.3500C>G MANE Select	ENSP00000259008.2:p.Ala1167Gly
ENST00000259008.6:c.3500C>G	ENSP00000259008.2:p.Ala1167Gly
NM_032043.2:c.3500C>G , LRG_300t1:c.3500C>G	NP_114432.2:p.Ala1167Gly
XM_011525332.1:c.3560C>G	XP_011523634.1:p.Ala1187Gly
XM_011525333.1:c.3560C>G	XP_011523635.1:p.Ala1187Gly
XM_011525334.1:c.3560C>G	XP_011523636.1:p.Ala1187Gly
XM_011525335.1:c.3500C>G	XP_011523637.1:p.Ala1167Gly
XM_011525336.1:c.3440C>G	XP_011523638.1:p.Ala1147Gly
XM_011525337.1:c.3359C>G	XP_011523639.1:p.Ala1120Gly
XM_011525338.1:c.3077C>G	XP_011523640.1:p.Ala1026Gly
XM_011525332.3:c.3560C>G	XP_011523634.1:p.Ala1187Gly
XM_011525333.3:c.3560C>G	XP_011523635.1:p.Ala1187Gly
XM_011525334.2:c.3560C>G	XP_011523636.1:p.Ala1187Gly
XM_011525335.3:c.3500C>G	XP_011523637.1:p.Ala1167Gly
XM_011525336.2:c.3440C>G	XP_011523638.1:p.Ala1147Gly
XM_011525337.2:c.3359C>G	XP_011523639.1:p.Ala1120Gly
XM_011525338.2:c.3077C>G	XP_011523640.1:p.Ala1026Gly
XM_017025200.1:c.3017C>G	XP_016880689.1:p.Ala1006Gly
XM_017025201.1:c.3017C>G	XP_016880690.1:p.Ala1006Gly
XM_017025202.1:c.1646C>G	XP_016880691.1:p.Ala549Gly
XM_017025203.1:c.1646C>G	XP_016880692.1:p.Ala549Gly
NM_032043.3:c.3500C>G MANE Select	NP_114432.2:p.Ala1167Gly