Canonical Allele Identifier: CA8690371

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 461146
• ClinVar RCV Id: RCV000554552 ; RCV001182277
• dbSNP Id: rs748140041
• ExAC: 17:59761102 T / C
• gnomAD v2: 17-59761102-T-C
• gnomAD v4: 17-61683741-T-C
• MyVariant Identifiers: chr17:g.59761102T>C (hg19) ; chr17:g.61683741T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683741T>C , CM000679.2:g.61683741T>C	GRCh38
NC_000017.10:g.59761102T>C , CM000679.1:g.59761102T>C	GRCh37
NC_000017.9:g.57115884T>C	NCBI36
NG_007409.2:g.184819A>G , LRG_300:g.184819A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2045A>G
ENST00000682453.1:c.3305A>G	ENSP00000506943.1:p.Asp1102Gly
ENST00000682477.1:c.*2731A>G	ENSP00000507075.1:n.*2731A>G
ENST00000682589.1:n.9182A>G
ENST00000682755.1:c.3083A>G	ENSP00000507660.1:p.Asp1028Gly
ENST00000682989.1:c.*396A>G	ENSP00000507786.1:n.*396A>G
ENST00000683039.1:c.3305A>G	ENSP00000508303.1:p.Asp1102Gly
ENST00000683235.1:c.*720A>G	ENSP00000507646.1:n.*720A>G
ENST00000683535.1:n.1435A>G
ENST00000684584.1:c.2468A>G	ENSP00000508044.1:p.Asp823Gly
ENST00000684626.1:n.1551A>G
ENST00000684769.1:c.1495A>G	ENSP00000507691.1:n.1495A>G
ENST00000259008.7:c.3305A>G MANE Select	ENSP00000259008.2:p.Asp1102Gly
ENST00000259008.6:c.3305A>G	ENSP00000259008.2:p.Asp1102Gly
NM_032043.2:c.3305A>G , LRG_300t1:c.3305A>G	NP_114432.2:p.Asp1102Gly
XM_011525332.1:c.3365A>G	XP_011523634.1:p.Asp1122Gly
XM_011525333.1:c.3365A>G	XP_011523635.1:p.Asp1122Gly
XM_011525334.1:c.3365A>G	XP_011523636.1:p.Asp1122Gly
XM_011525335.1:c.3305A>G	XP_011523637.1:p.Asp1102Gly
XM_011525336.1:c.3245A>G	XP_011523638.1:p.Asp1082Gly
XM_011525337.1:c.3164A>G	XP_011523639.1:p.Asp1055Gly
XM_011525338.1:c.2882A>G	XP_011523640.1:p.Asp961Gly
XM_011525332.3:c.3365A>G	XP_011523634.1:p.Asp1122Gly
XM_011525333.3:c.3365A>G	XP_011523635.1:p.Asp1122Gly
XM_011525334.2:c.3365A>G	XP_011523636.1:p.Asp1122Gly
XM_011525335.3:c.3305A>G	XP_011523637.1:p.Asp1102Gly
XM_011525336.2:c.3245A>G	XP_011523638.1:p.Asp1082Gly
XM_011525337.2:c.3164A>G	XP_011523639.1:p.Asp1055Gly
XM_011525338.2:c.2882A>G	XP_011523640.1:p.Asp961Gly
XM_017025200.1:c.2822A>G	XP_016880689.1:p.Asp941Gly
XM_017025201.1:c.2822A>G	XP_016880690.1:p.Asp941Gly
XM_017025202.1:c.1451A>G	XP_016880691.1:p.Asp484Gly
XM_017025203.1:c.1451A>G	XP_016880692.1:p.Asp484Gly
NM_032043.3:c.3305A>G MANE Select	NP_114432.2:p.Asp1102Gly