Canonical Allele Identifier: CA400478725

Gene: BRIP1

Linked Data

• dbSNP Id: rs2144076036
• MyVariant Identifiers: chr17:g.59760969T>A (hg19) ; chr17:g.61683608T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61683608T>A , CM000679.2:g.61683608T>A	GRCh38
NC_000017.10:g.59760969T>A , CM000679.1:g.59760969T>A	GRCh37
NC_000017.9:g.57115751T>A	NCBI36
NG_007409.2:g.184952A>T , LRG_300:g.184952A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682073.1:n.2178A>T
ENST00000682453.1:c.3438A>T	ENSP00000506943.1:p.Lys1146Asn
ENST00000682477.1:c.*2864A>T	ENSP00000507075.1:n.*2864A>T
ENST00000682589.1:n.9315A>T
ENST00000682755.1:c.3216A>T	ENSP00000507660.1:p.Lys1072Asn
ENST00000682989.1:c.*529A>T	ENSP00000507786.1:n.*529A>T
ENST00000683039.1:c.3438A>T	ENSP00000508303.1:p.Lys1146Asn
ENST00000683235.1:c.*853A>T	ENSP00000507646.1:n.*853A>T
ENST00000683535.1:n.1568A>T
ENST00000684584.1:c.2601A>T	ENSP00000508044.1:p.Lys867Asn
ENST00000684626.1:n.1684A>T
ENST00000684769.1:c.1628A>T	ENSP00000507691.1:n.1628A>T
ENST00000259008.7:c.3438A>T MANE Select	ENSP00000259008.2:p.Lys1146Asn
ENST00000259008.6:c.3438A>T	ENSP00000259008.2:p.Lys1146Asn
NM_032043.2:c.3438A>T , LRG_300t1:c.3438A>T	NP_114432.2:p.Lys1146Asn
XM_011525332.1:c.3498A>T	XP_011523634.1:p.Lys1166Asn
XM_011525333.1:c.3498A>T	XP_011523635.1:p.Lys1166Asn
XM_011525334.1:c.3498A>T	XP_011523636.1:p.Lys1166Asn
XM_011525335.1:c.3438A>T	XP_011523637.1:p.Lys1146Asn
XM_011525336.1:c.3378A>T	XP_011523638.1:p.Lys1126Asn
XM_011525337.1:c.3297A>T	XP_011523639.1:p.Lys1099Asn
XM_011525338.1:c.3015A>T	XP_011523640.1:p.Lys1005Asn
XM_011525332.3:c.3498A>T	XP_011523634.1:p.Lys1166Asn
XM_011525333.3:c.3498A>T	XP_011523635.1:p.Lys1166Asn
XM_011525334.2:c.3498A>T	XP_011523636.1:p.Lys1166Asn
XM_011525335.3:c.3438A>T	XP_011523637.1:p.Lys1146Asn
XM_011525336.2:c.3378A>T	XP_011523638.1:p.Lys1126Asn
XM_011525337.2:c.3297A>T	XP_011523639.1:p.Lys1099Asn
XM_011525338.2:c.3015A>T	XP_011523640.1:p.Lys1005Asn
XM_017025200.1:c.2955A>T	XP_016880689.1:p.Lys985Asn
XM_017025201.1:c.2955A>T	XP_016880690.1:p.Lys985Asn
XM_017025202.1:c.1584A>T	XP_016880691.1:p.Lys528Asn
XM_017025203.1:c.1584A>T	XP_016880692.1:p.Lys528Asn
NM_032043.3:c.3438A>T MANE Select	NP_114432.2:p.Lys1146Asn