Canonical Allele Identifier: CA400479924

Gene: BRIP1

Linked Data

• MyVariant Identifiers: chr17:g.59761362T>G (hg19) ; chr17:g.61684001T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61684001T>G , CM000679.2:g.61684001T>G	GRCh38
NC_000017.10:g.59761362T>G , CM000679.1:g.59761362T>G	GRCh37
NC_000017.9:g.57116144T>G	NCBI36
NG_007409.2:g.184559A>C , LRG_300:g.184559A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.1785A>C
ENST00000682453.1:c.3045A>C	ENSP00000506943.1:p.Lys1015Asn
ENST00000682477.1:c.*2471A>C	ENSP00000507075.1:n.*2471A>C
ENST00000682589.1:n.8922A>C
ENST00000682755.1:c.2823A>C	ENSP00000507660.1:p.Lys941Asn
ENST00000682989.1:c.*136A>C	ENSP00000507786.1:n.*136A>C
ENST00000683039.1:c.3045A>C	ENSP00000508303.1:p.Lys1015Asn
ENST00000683235.1:c.*460A>C	ENSP00000507646.1:n.*460A>C
ENST00000683535.1:n.1175A>C
ENST00000684584.1:c.2208A>C	ENSP00000508044.1:p.Lys736Asn
ENST00000684626.1:n.1291A>C
ENST00000684769.1:c.1235A>C	ENSP00000507691.1:n.1235A>C
ENST00000259008.7:c.3045A>C MANE Select	ENSP00000259008.2:p.Lys1015Asn
ENST00000259008.6:c.3045A>C	ENSP00000259008.2:p.Lys1015Asn
NM_032043.2:c.3045A>C , LRG_300t1:c.3045A>C	NP_114432.2:p.Lys1015Asn
XM_011525332.1:c.3105A>C	XP_011523634.1:p.Lys1035Asn
XM_011525333.1:c.3105A>C	XP_011523635.1:p.Lys1035Asn
XM_011525334.1:c.3105A>C	XP_011523636.1:p.Lys1035Asn
XM_011525335.1:c.3045A>C	XP_011523637.1:p.Lys1015Asn
XM_011525336.1:c.2985A>C	XP_011523638.1:p.Lys995Asn
XM_011525337.1:c.2904A>C	XP_011523639.1:p.Lys968Asn
XM_011525338.1:c.2622A>C	XP_011523640.1:p.Lys874Asn
XM_011525332.3:c.3105A>C	XP_011523634.1:p.Lys1035Asn
XM_011525333.3:c.3105A>C	XP_011523635.1:p.Lys1035Asn
XM_011525334.2:c.3105A>C	XP_011523636.1:p.Lys1035Asn
XM_011525335.3:c.3045A>C	XP_011523637.1:p.Lys1015Asn
XM_011525336.2:c.2985A>C	XP_011523638.1:p.Lys995Asn
XM_011525337.2:c.2904A>C	XP_011523639.1:p.Lys968Asn
XM_011525338.2:c.2622A>C	XP_011523640.1:p.Lys874Asn
XM_017025200.1:c.2562A>C	XP_016880689.1:p.Lys854Asn
XM_017025201.1:c.2562A>C	XP_016880690.1:p.Lys854Asn
XM_017025202.1:c.1191A>C	XP_016880691.1:p.Lys397Asn
XM_017025203.1:c.1191A>C	XP_016880692.1:p.Lys397Asn
NM_032043.3:c.3045A>C MANE Select	NP_114432.2:p.Lys1015Asn