Canonical Allele Identifier: CA400478409

Gene: BRIP1

Linked Data

• ClinVar Variation Id: 2306679
• ClinVar RCV Id: RCV004153281
• dbSNP Id: rs2144072945
• MyVariant Identifiers: chr17:g.59760880A>G (hg19) ; chr17:g.61683519A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683519A>G , CM000679.2:g.61683519A>G	GRCh38
NC_000017.10:g.59760880A>G , CM000679.1:g.59760880A>G	GRCh37
NC_000017.9:g.57115662A>G	NCBI36
NG_007409.2:g.185041T>C , LRG_300:g.185041T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2267T>C
ENST00000682453.1:c.3527T>C	ENSP00000506943.1:p.Ile1176Thr
ENST00000682477.1:c.*2953T>C	ENSP00000507075.1:n.*2953T>C
ENST00000682589.1:n.9404T>C
ENST00000682755.1:c.3305T>C	ENSP00000507660.1:p.Ile1102Thr
ENST00000682989.1:c.*618T>C	ENSP00000507786.1:n.*618T>C
ENST00000683039.1:c.3527T>C	ENSP00000508303.1:p.Ile1176Thr
ENST00000683235.1:c.*942T>C	ENSP00000507646.1:n.*942T>C
ENST00000683535.1:n.1657T>C
ENST00000684584.1:c.2690T>C	ENSP00000508044.1:p.Ile897Thr
ENST00000684626.1:n.1773T>C
ENST00000684769.1:c.1717T>C	ENSP00000507691.1:n.1717T>C
ENST00000259008.7:c.3527T>C MANE Select	ENSP00000259008.2:p.Ile1176Thr
ENST00000259008.6:c.3527T>C	ENSP00000259008.2:p.Ile1176Thr
NM_032043.2:c.3527T>C , LRG_300t1:c.3527T>C	NP_114432.2:p.Ile1176Thr
XM_011525332.1:c.3587T>C	XP_011523634.1:p.Ile1196Thr
XM_011525333.1:c.3587T>C	XP_011523635.1:p.Ile1196Thr
XM_011525334.1:c.3587T>C	XP_011523636.1:p.Ile1196Thr
XM_011525335.1:c.3527T>C	XP_011523637.1:p.Ile1176Thr
XM_011525336.1:c.3467T>C	XP_011523638.1:p.Ile1156Thr
XM_011525337.1:c.3386T>C	XP_011523639.1:p.Ile1129Thr
XM_011525338.1:c.3104T>C	XP_011523640.1:p.Ile1035Thr
XM_011525332.3:c.3587T>C	XP_011523634.1:p.Ile1196Thr
XM_011525333.3:c.3587T>C	XP_011523635.1:p.Ile1196Thr
XM_011525334.2:c.3587T>C	XP_011523636.1:p.Ile1196Thr
XM_011525335.3:c.3527T>C	XP_011523637.1:p.Ile1176Thr
XM_011525336.2:c.3467T>C	XP_011523638.1:p.Ile1156Thr
XM_011525337.2:c.3386T>C	XP_011523639.1:p.Ile1129Thr
XM_011525338.2:c.3104T>C	XP_011523640.1:p.Ile1035Thr
XM_017025200.1:c.3044T>C	XP_016880689.1:p.Ile1015Thr
XM_017025201.1:c.3044T>C	XP_016880690.1:p.Ile1015Thr
XM_017025202.1:c.1673T>C	XP_016880691.1:p.Ile558Thr
XM_017025203.1:c.1673T>C	XP_016880692.1:p.Ile558Thr
NM_032043.3:c.3527T>C MANE Select	NP_114432.2:p.Ile1176Thr